US Code
Title 21— FOOD AND DRUGS

§ 16. Introduction into, or sale in, State or Territory or District of Columbia of dairy or food products falsely labeled or branded - No person or persons, company or corporation, shall introduce into...

§ 17. Penalty for sale or introduction of falsely labeled dairy or food products; venue - If any person or persons violate the provisions of ,...

§ 18. Suspension of importation of adulterated articles - Whenever the President is satisfied that there is good reason...

§ 19. Repealed. , -

§ 20. Apples in interstate commerce; standard grades - The standard grades for apples when packed in barrels which...

§ 21. Branding grades on barrels of apples - The barrels in which apples are packed in accordance with...

§ 22. Barrels misbranded - Barrels packed with apples shall be deemed to be misbranded...

§ 23. Penalties - Any person, firm or corporation, or association who shall knowingly...

§ 24. Omitted -

§ 25. Oleomargarine, butterine, or imitation butter or cheese transported into a State subject to its police powers - All articles known as oleomargarine, butterine, imitation, process, renovated, or...

§ 26. Omitted -

CHAPTER 2— TEAS

§§ 41 to 50. Repealed. , , -

CHAPTER 3— FILLED MILK

§ 61. Definitions - (a) The term “person” includes an individual, partnership, corporation, or...

§ 62. Manufacture, shipment, or delivery for shipment in interstate or foreign commerce prohibited - It is declared that filled milk, as defined in ,...

§ 63. Penalties; acts of agents deemed acts of principals - Any person violating any provision of this chapter shall upon...

§ 64. Regulations for enforcement - The Secretary of Health and Human Services is authorized and...

CHAPTER 4— ANIMALS, MEATS, AND MEAT AND DAIRY PRODUCTS

SUBCHAPTER I— EXAMINATION OF ANIMALS, MEATS, AND MEAT AND DAIRY PRODUCTS

§§ 71 to 92. Transferred -

§ 93. Repealed. , -

§§ 94 to 95. Transferred -

§ 96. Repealed. , , -

§§ 97 to 97d. Omitted -

§ 98. Transferred -

§ 99. Repealed. , title I, § 101, -

SUBCHAPTER II— IMPORTATION OF CATTLE AND QUARANTINE

§ 101. Suspension of importation of all animals - Whenever, in the opinion of the President, it shall be...

§§ 102 to 105. Repealed. , , -

§§ 106, 107. Omitted -

SUBCHAPTER III— PREVENTION OF INTRODUCTION AND SPREAD OF CONTAGION

§§ 111, 112. Repealed. , (8), , , 508 -

§ 112a. Omitted -

§ 113. Repealed. , (8), , , 508 -

§ 113a. Establishment of research laboratories for foot-and-mouth disease and other animal diseases; research contracts; employment of technicians and scientists; appropriations - The Secretary of Agriculture is authorized to establish research laboratories,...

§§ 114 to 114d–1. Repealed. , (9), , -

§§ 114d–2 to 114d–6. Repealed. , , -

§§ 114e to 114h. Repealed. , (11), , -

§ 114i. Pseudorabies eradication - (a) FindingsCongress finds that efforts to eradicate pseudorabies in United...

§§ 115 to 128. Repealed. , (8), (12)–(14), , , 508 -

§ 129. Omitted -

§§ 129a to 131. Repealed. , (8), (16), , , 508 -

§ 132. Transferred -

§ 133. Repealed. , -

§§ 134 to 135b. Repealed. , (18), , -

§ 136. Additional inspection services - The Secretary of Agriculture, in carrying out regulations prohibiting or...

§ 136a. Collection of fees for inspection services - (a) Quarantine and inspection fees(1) Fees authorizedThe Secretary of Agriculture...

SUBCHAPTER IV— IMPORTATION OF MILK AND CREAM

§ 141. Prohibition of importation without permit - On and after , the importation into the United States...

§ 142. Milk or cream when unfit for importation - Milk or cream shall be considered unfit for importation (1)...

§ 143. Inspection; certified statement in lieu thereof; waiver of requirements of section 142; regulations; suspension and revocation of permits - The Secretary of Health and Human Services shall cause such...

§ 144. Unlawful receiving of imported milk or cream - It shall be unlawful for any person in the United...

§ 145. Penalties - Any person who knowingly violates any provision of this subchapter...

§ 146. Authorization of appropriations - There is authorized to be appropriated, out of any moneys...

§ 147. Repeal of inconsistent laws - Any laws or parts of laws inconsistent with this subchapter...

§ 148. Powers of State with respect to milk or cream lawfully imported - Nothing in this subchapter is intended nor shall be construed...

§ 149. Definitions - (a) The term “person” means an individual, partnership, association, or...

CHAPTER 5— VIRUSES, SERUMS, TOXINS, ANTITOXINS, AND ANALOGOUS PRODUCTS

§ 151. Preparation and sale of worthless or harmful products for domestic animals prohibited; preparation to be in compliance with rules at licensed establishments - It shall be unlawful for any person, firm, or corporation...

§ 152. Importation regulated and prohibited - The importation into the United States of any virus, serum,...

§ 153. Inspection of imports; denial of entry and destruction - The Secretary of Agriculture is authorized to cause the Bureau...

§ 154. Regulations for preparation and sale; licenses - The Secretary of Agriculture is authorized to make and promulgate...

§ 154a. Special licenses for special circumstances; expedited procedure; conditions; exemptions; criteria - (1) solely for administration to animals of such person, firm,...

§ 155. Permits for importation - The Secretary of Agriculture is authorized to issue permits for...

§ 156. Licenses conditioned on permitting inspection; suspension of licenses - All licenses issued under authority of this chapter to establishments...

§ 157. Inspection - Any officer, agent, or employee of the Department of Agriculture...

§ 158. Offenses; punishment - Any person, firm, or corporation who shall violate any of...

§ 159. Enforcement; penalties applicable; Congressional findings - The procedures of sections 672, 673, and 674 of this...

CHAPTER 5A— BUREAU OF NARCOTICS

§§ 161 to 165. Omitted -

CHAPTER 6— NARCOTIC DRUGS -

CHAPTER 7— PRACTICE OF PHARMACY AND SALE OF POISONS IN CONSULAR DISTRICTS IN CHINA

§ 201. Doing business without a license unlawful; employment of Chinese subjects - It shall be unlawful in the consular districts of the...

§ 202. Certain classes of persons and corporations excepted; insecticides - Nothing in shall be construed to interfere with any recognized...

§ 203. Application for license; requirements; qualifications for license - Every person whose permanent allegiance is due to the United...

§ 204. Issuance of license - If the applicant for license as a pharmacist has complied...

§ 205. Display of license in pharmacy - Every license to practice pharmacy shall be conspicuously displayed by...

§ 206. Revocation of license - The license of any person whose permanent allegiance is due...

§ 207. Restrictions on sales; written orders or prescriptions - It shall be unlawful for any person, firm, or corporation...

§ 208. Certain preparations and sales excepted - The provisions of shall not apply to preparations containing not...

§ 209. Poisons; book entry of sale; labels - It shall be unlawful for any person, firm, or corporation...

§ 210. Pharmacist; unauthorized use of title - It shall be unlawful for any person whose permanent allegiance...

§ 211. Preservation of originals of prescriptions compounded and copies thereof; inspection of prescriptions by consular officers; marking containers of drugs - Every person, firm, or corporation whose permanent allegiance is due...

§ 212. Offenses; punishment; duty to enforce provisions - Any person, firm, or corporation, whose permanent allegiance is due...

§ 213. Fraudulent representations to evade or defeat restrictions - No person, firm, or corporation whose permanent allegiance is due...

§ 214. Previous laws unaffected - Nothing in this chapter shall be construed as modifying or...

§ 215. “Consul” defined - The word “consul” as used in this chapter shall mean...

CHAPTER 8— NARCOTIC FARMS

§§ 221 to 237. Repealed. , title XIII, § 1313, -

CHAPTER 9— FEDERAL FOOD, DRUG, AND COSMETIC ACT

SUBCHAPTER I— SHORT TITLE

§ 301. Short title - This chapter may be cited as the Federal Food, Drug,...

SUBCHAPTER II— DEFINITIONS

§ 321. Definitions; generally - (a)(1) The term “State”, except as used in the last...

§ 321a. “Butter” defined - For the purposes of the Food and Drug Act of...

§ 321b. “Package” defined - The word “package” where it occurs the second and last...

§ 321c. Nonfat dry milk; “milk” defined - For the purposes of the Federal Food, Drug, and Cosmetic...

§ 321d. Market names for catfish and ginseng - (a) Catfish labeling(1) In generalNotwithstanding any other provision of law,...

SUBCHAPTER III— PROHIBITED ACTS AND PENALTIES

§ 331. Prohibited acts - (a) The introduction or delivery for introduction into interstate commerce...

§ 332. Injunction proceedings - (a) Jurisdiction of courtsThe district courts of the United States...

§ 333. Penalties - (a) Violation of section 331 of this title; second violation;...

§ 333a. Repealed. , , -

§ 334. Seizure - (a) Grounds and jurisdiction(1) Any article of food, drug, or...

§ 335. Hearing before report of criminal violation - Before any violation of this chapter is reported by the...

§ 335a. Debarment, temporary denial of approval, and suspension - (a) Mandatory debarment; certain drug applications(1) Corporations, partnerships, and associationsIf...

§ 335b. Civil penalties - (a) In generalAny person that the Secretary finds—(1) knowingly made...

§ 335c. Authority to withdraw approval of abbreviated drug applications - (a) In generalThe Secretary—(1) shall withdraw approval of an abbreviated...

§ 336. Report of minor violations - Nothing in this chapter shall be construed as requiring the...

§ 337. Proceedings in name of United States; provision as to subpoenas - (a) Except as provided in subsection (b), all such proceedings...

§ 337a. Extraterritorial jurisdiction - There is extraterritorial jurisdiction over any violation of this chapter...

SUBCHAPTER IV— FOOD

§ 341. Definitions and standards for food - Whenever in the judgment of the Secretary such action will...

§ 342. Adulterated food - (a) Poisonous, insanitary, etc., ingredients(1) If it bears or contains...

§ 343. Misbranded food - (a) False or misleading labelIf (1) its labeling is false...

§ 343–1. National uniform nutrition labeling - (a) Except as provided in subsection (b), no State or...

§ 343–2. Dietary supplement labeling exemptions - (a) In generalA publication, including an article, a chapter in...

§ 343–3. Disclosure - (a) No provision of section 321(n), 343(a), or 348 of...

§ 343a. Repealed. , , , 2763A–73 -

§ 344. Emergency permit control - (a) Conditions on manufacturing, processing, etc., as health measureWhenever the...

§ 345. Regulations making exemptions - The Secretary shall promulgate regulations exempting from any labeling requirement...

§ 346. Tolerances for poisonous or deleterious substances in food; regulations - Any poisonous or deleterious substance added to any food, except...

§ 346a. Tolerances and exemptions for pesticide chemical residues - (a) Requirement for tolerance or exemption(1) General ruleExcept as provided...

§ 346b. Authorization of appropriations - There are authorized to be appropriated, out of any moneys...

§ 347. Intrastate sales of colored oleomargarine - (a) Law governingColored oleomargarine or colored margarine which is sold...

§ 347a. Congressional declaration of policy regarding oleomargarine sales - The Congress hereby finds and declares that the sale, or...

§ 347b. Contravention of State laws - Nothing in this Act shall be construed as authorizing the...

§ 348. Food additives - (a) Unsafe food additives; exception for conformity with exemption or...

§ 349. Bottled drinking water standards; publication in Federal Register - (a) Except as provided in subsection (b), whenever the Administrator...

§ 350. Vitamins and minerals - (a) Authority and limitations of Secretary; applicability(1) Except as provided...

§ 350a. Infant formulas - (a) AdulterationAn infant formula, including an infant formula powder, shall...

§ 350a–1. Protecting infants and improving formula supply - (a) Definitions(1) In generalIn this section, the term “infant formula”...

§ 350b. New dietary ingredients - (a) In generalA dietary supplement which contains a new dietary...

§ 350c. Maintenance and inspection of records - (a) Records inspection(1) Adulterated foodIf the Secretary has a reasonable...

§ 350d. Registration of food facilities - (a) Registration(1) In generalThe Secretary shall by regulation require that...

§ 350e. Sanitary transportation practices - (a) DefinitionsIn this section:(1) Bulk vehicleThe term “bulk vehicle” includes...

§ 350f. Reportable food registry - (a) DefinitionsIn this section:(1) Responsible partyThe term “responsible party”, with...

§ 350g. Hazard analysis and risk-based preventive controls - (a) In generalThe owner, operator, or agent in charge of...

§ 350h. Standards for produce safety - (a) Proposed rulemaking(1) In general(A) RulemakingNot later than 1 year...

§ 350i. Protection against intentional adulteration - (a) Determinations(1) In generalThe Secretary shall—(A) conduct a vulnerability assessment...

§ 350j. Targeting of inspection resources for domestic facilities, foreign facilities, and ports of entry; annual report - (a) Identification and inspection of facilities(1) IdentificationThe Secretary shall identify...

§ 350k. Laboratory accreditation for analyses of foods - (a) Recognition of laboratory accreditation(1) In generalNot later than 2...

§ 350l. Mandatory recall authority - (a) Voluntary proceduresIf the Secretary determines, based on information gathered...

§ 350l–1. Annual report to Congress - (1) In generalNot later than 2 years after January 4,...

§ 350m. Requirements for critical food - (a) Notification of meaningful disruption for critical food(1) In generalA...

SUBCHAPTER V— DRUGS AND DEVICES

Part A— Drugs and Devices

§ 351. Adulterated drugs and devices - (a) Poisonous, insanitary, etc., ingredients; adequate controls in manufacture(1) If...

§ 352. Misbranded drugs and devices - (a) False or misleading label(1) If its labeling is false...

§ 353. Exemptions and consideration for certain drugs, devices, and biological products - (a) Regulations for goods to be processed, labeled, or repacked...

§ 353a. Pharmacy compounding - (a) In generalSections 351(a)(2)(B), 352(f)(1), and 355 of this title...

§ 353a–1. Enhanced communication - (a) Submissions from State boards of pharmacyIn a manner specified...

§ 353b. Outsourcing facilities - (a) In generalSections 352(f)(1), 355, and 360eee–1 of this title...

§ 353c. Prereview of television advertisements - (a) In generalThe Secretary may require the submission of any...

§ 353d. Process to update labeling for certain generic drugs - (a) DefinitionsFor purposes of this section:(1) The term “covered drug”...

§ 354. Veterinary feed directive drugs - (a) Lawful veterinary feed directive requirement(1) A drug intended for...

§ 355. New drugs - (a) Necessity of effective approval of applicationNo person shall introduce...

§ 355–1. Risk evaluation and mitigation strategies - (a) Submission of proposed strategy(1) Initial approvalIf the Secretary, in...

§ 355–2. Actions for delays of generic drugs and biosimilar biological products - (a) DefinitionsIn this section—(1) the term “commercially reasonable, market-based terms”...

§ 355a. Pediatric studies of drugs - (a) DefinitionsAs used in this section, the term “pediatric studies”...

§ 355b. Adverse-event reporting - (a) Toll-free number in labelingNot later than one year after...

§ 355c. Research into pediatric uses for drugs and biological products - (a) New drugs and biological products(1) In general(A) General requirementsExcept...

§ 355c–1. Report - (a) In generalNot later than four years after July 9,...

§ 355d. Internal committee for review of pediatric plans, assessments, deferrals, deferral extensions, and waivers - The Secretary shall establish an internal committee within the Food...

§ 355e. Pharmaceutical security - (a) In generalThe Secretary shall develop standards and identify and...

§ 355f. Extension of exclusivity period for new qualified infectious disease products - (a) ExtensionIf the Secretary approves an application pursuant to section...

§ 355g. Utilizing real world evidence - (a) In generalThe Secretary shall establish a program to evaluate...

§ 355h. Regulation of certain nonprescription drugs that are marketed without an approved drug application - (a) Nonprescription drugs marketed without an approved applicationNonprescription drugs marketed...

§ 356. Expedited approval of drugs for serious or life-threatening diseases or conditions - (a) Designation of a drug as a breakthrough therapy(1) In...

§ 356–1. Accelerated approval of priority countermeasures - (a) In generalThe Secretary of Health and Human Services may...

§ 356–2. Accelerated approval Council - (1) In generalNot later than 1 year after December 29,...

§ 356a. Manufacturing changes - (a) In generalWith respect to a drug for which there...

§ 356b. Reports of postmarketing studies - (a) Submission(1) In generalA sponsor of a drug that has...

§ 356c. Discontinuance or interruption in the production of life-saving drugs - (a) In generalA manufacturer of a drug—(1) that is—(A) life-supporting;...

§ 356c–1. Annual reporting on drug shortages - (a) Annual reports to CongressNot later than March 31 of...

§ 356d. Coordination; task force and strategic plan - (a) Task force and strategic plan(1) In general(A) Task forceAs...

§ 356e. Drug shortage list - (a) EstablishmentThe Secretary shall maintain an up-to-date list of drugs...

§ 356f. Hospital repackaging of drugs in shortage - (a) DefinitionsIn this section:(1) DrugThe term “drug” excludes any controlled...

§ 356g. Standards for regenerative medicine and regenerative advanced therapies - (a) In generalNot later than 2 years after December 13,...

§ 356h. Competitive generic therapies - (a) In generalThe Secretary may, at the request of an...

§ 356i. Prompt reports of marketing status - (a) Notification of withdrawalThe holder of an application approved under...

§ 356j. Discontinuance or interruption in the production of medical devices - (a) In generalA manufacturer of a device that—(1) is critical...

§ 356k. Platform technologies - (a) In generalThe Secretary shall establish a program for the...

§ 356l. Advanced manufacturing technologies designation program - (a) In generalNot later than 1 year after December 29,...

§ 357. Qualification of drug development tools - (a) Process for qualification(1) In generalThe Secretary shall establish a...

§ 358. Authority to designate official names - (a) Necessity or desirability; use in official compendiums; infringement of...

§ 359. Nonapplicability of subchapter to cosmetics - This subchapter, as amended by the Drug Amendments of 1962,...

§ 360. Registration of producers of drugs or devices - (a) DefinitionsAs used in this section—(1) the term “manufacture, preparation,...

§ 360a. Clinical trial guidance for antibiotic drugs - (a) In generalNot later than 1 year after September 27,...

§ 360a–1. Clinical trials - (a) Review and revision of guidance documents(1) In generalThe Secretary...

§ 360a–2. Susceptibility test interpretive criteria for microorganisms - (a) Purpose; identification of criteria(1) PurposeThe purpose of this section...

§ 360b. New animal drugs - (a) Unsafe new animal drugs and animal feed containing such...

§ 360b–1. Priority zoonotic animal drugs - (a) In generalThe Secretary shall, at the request of the...

§ 360c. Classification of devices intended for human use - (a) Classes of devices(1) There are established the following classes...

§ 360c–1. Reporting - (1) the number and type of class I and class...

§ 360d. Performance standards - (a) Reasonable assurance of safe and effective performance; periodic evaluation(1)...

§ 360e. Premarket approval - (a) General requirementA class III device—(1) which is subject to...

§ 360e–1. Pediatric uses of devices - (a) New devices(1) In generalA person that submits to the...

§ 360e–3. Breakthrough devices - (a) PurposeThe purpose of this section is to encourage the...

§ 360e–4. Predetermined change control plans for devices - (a) Approved devices(1) In generalNotwithstanding section 360e(d)(5)(A) of this title,...

§ 360f. Banned devices - (a) General ruleWhenever the Secretary finds, on the basis of...

§ 360g. Judicial review - (a) Petition; recordNot later than thirty days after—(1) the promulgation...

§ 360g–1. Agency documentation and review of significant decisions regarding devices - (a) Documentation of rationale for significant decisions(1) In generalThe Secretary...

§ 360g–2. Third party data transparency - (a) In generalTo the extent the Secretary relies on any...

§ 360h. Notification and other remedies - (a) NotificationIf the Secretary determines that—(1) a device intended for...

§ 360h–1. Program to improve the device recall system - (a) In generalThe Secretary shall—(1) establish a program to routinely...

§ 360i. Records and reports on devices - (a) General ruleEvery person who is a manufacturer or importer...

§ 360j. General provisions respecting control of devices intended for human use - (a) General ruleAny requirement authorized by or under section 351,...

§ 360k. State and local requirements respecting devices - (a) General ruleExcept as provided in subsection (b), no State...

§ 360l. Postmarket surveillance - (a) Postmarket surveillance(1) In general(A) ConductThe Secretary may by order,...

§ 360m. Accredited persons - (a) In general(1) Review and classification of devicesNot later than...

§ 360n. Priority review to encourage treatments for tropical diseases - (a) DefinitionsIn this section:(1) Priority reviewThe term “priority review”, with...

§ 360n–1. Priority review for qualified infectious disease products - (a) In generalIf the Secretary designates a drug under section...

§ 360n–2. Ensuring cybersecurity of devices - (a) In generalA person who submits an application or submission...

Part B— Drugs for Rare Diseases or Conditions

§ 360aa. Recommendations for investigations of drugs for rare diseases or conditions - (a) Request by sponsor; response by SecretaryThe sponsor of a...

§ 360bb. Designation of drugs for rare diseases or conditions - (a) Request by sponsor; preconditions; “rare disease or condition” defined(1)...

§ 360cc. Protection for drugs for rare diseases or conditions - (a) Exclusive approval, certification, or licenseExcept as provided in subsection...

§ 360dd. Open protocols for investigations of drugs for rare diseases or conditions - If a drug is designated under as a drug for...

§ 360ee. Grants and contracts for development of drugs for rare diseases and conditions - (a) Authority of SecretaryThe Secretary may make grants to and...

§ 360ee–1. FDA rare neurodegenerative disease grant program - (1) to characterize such neurodegenerative diseases and their natural history;...

§ 360ff. Priority review to encourage treatments for rare pediatric diseases - (a) DefinitionsIn this section:(1) Priority reviewThe term “priority review”, with...

§ 360ff–1. Targeted drugs for rare diseases - (a) PurposeThe purpose of this section, through the approach provided...

Part C— Electronic Product Radiation Control

§ 360hh. Definitions - (1) the term “electronic product radiation” means—(A) any ionizing or...

§ 360ii. Program of control - (a) EstablishmentThe Secretary shall establish and carry out an electronic...

§ 360jj. Studies by Secretary - (a) Report to CongressThe Secretary shall conduct the following studies,...

§ 360kk. Performance standards for electronic products - (a) Promulgation of regulations(1) The Secretary shall by regulation prescribe...

§ 360ll. Notification of defects in and repair or replacement of electronic products - (a) Notification; exemption(1) Every manufacturer of electronic products who discovers...

§ 360mm. Imports - (a) Refusal of admission to noncomplying electronic productsAny electronic product...

§ 360nn. Inspection, records, and reports - (a) Inspection of premisesIf the Secretary finds for good cause...

§ 360oo. Prohibited acts - (a) It shall be unlawful—(1) for any manufacturer to introduce,...

§ 360pp. Enforcement - (a) Jurisdiction of courtsThe district courts of the United States...

§ 360qq. Repealed. , , -

§ 360rr. Federal-State cooperation - The Secretary is authorized (1) to accept from State and...

§ 360ss. State standards - Whenever any standard prescribed pursuant to with respect to an...

Part D— Dissemination of Treatment Information

§§ 360aaa to 360aaa–6. Omitted -

Part E— General Provisions Relating to Drugs and Devices

§ 360bbb. Expanded access to unapproved therapies and diagnostics - (a) Emergency situationsThe Secretary may, under appropriate conditions determined by...

§ 360bbb–0. Expanded access policy required for investigational drugs - (a) In generalThe manufacturer or distributor of one or more...

§ 360bbb–0a. Investigational drugs for use by eligible patients - (a) DefinitionsFor purposes of this section—(1) the term “eligible patient”...

§ 360bbb–1. Dispute resolution - If, regarding an obligation concerning drugs or devices under this...

§ 360bbb–2. Classification of products - (a) RequestA person who submits an application or submission (including...

§ 360bbb–3. Authorization for medical products for use in emergencies - (a) In general(1) Emergency usesNotwithstanding any provision of this chapter...

§ 360bbb–3a. Emergency use of medical products - (a) DefinitionsIn this section:(1) Eligible productThe term “eligible product” means...

§ 360bbb–3b. Products held for emergency use - (1) is intended to be held and not used; and...

§ 360bbb–3c. Expedited development and review of medical products for emergency uses - (1) In generalThe Secretary of Defense may request that the...

§ 360bbb–4. Countermeasure development, review, and technical assistance - (a) DefinitionsIn this section—(1) the term “countermeasure” means a qualified...

§ 360bbb–4a. Priority review to encourage treatments for agents that present national security threats - (a) DefinitionsIn this section:(1) Human drug applicationThe term “human drug...

§ 360bbb–4b. Medical countermeasure master files - (a) Applicability of reference(1) In generalA person may submit data...

§ 360bbb–5. Critical Path Public-Private Partnerships - (a) EstablishmentThe Secretary, acting through the Commissioner of Food and...

§ 360bbb–5a. Emerging technology program - (a) Program establishment(1) In generalThe Secretary shall establish a program...

§ 360bbb–6. Risk communication - (a) Advisory Committee on Risk Communication(1) In generalThe Secretary shall...

§ 360bbb–7. Notification - (a) Notification to SecretaryWith respect to a drug, the Secretary...

§ 360bbb–8. Consultation with external experts on rare diseases, targeted therapies, and genetic targeting of treatments - (a) In generalFor the purpose of promoting the efficiency of...

§ 360bbb–8a. Optimizing global clinical trials - (a) In generalThe Secretary shall—(1) work with other regulatory authorities...

§ 360bbb–8b. Use of clinical investigation data from outside the United States - (a) In generalIn determining whether to approve, license, or clear...

§ 360bbb–8c. Patient participation in medical product discussion - (a) Patient engagement in drugs and devices(1) In generalThe Secretary...

§ 360bbb–8d. Notification, nondistribution, and recall of controlled substances - (a) Order to cease distribution and recall(1) In generalIf the...

Part F— New Animal Drugs for Minor Use and Minor Species

§ 360ccc. Conditional approval of new animal drugs for minor use and minor species and certain new animal drugs - (a) Application requirements(1)(A) Except as provided in paragraph (3), any...

§ 360ccc–1. Index of legally marketed unapproved new animal drugs for minor species - (a) Establishment and content(1) The Secretary shall establish an index...

§ 360ccc–2. Designated new animal drugs for minor use or minor species - (a) Designation(1) The manufacturer or the sponsor of a new...

Part G— Medical Gases

§ 360ddd. Definitions - (1) The term “designated medical gas” means any of the...

§ 360ddd–1. Regulation of medical gases - (a) Certification of designated medical gases(1) SubmissionBeginning 180 days after...

§ 360ddd–2. Inapplicability of drug fees to designated medical gases - A designated medical gas, alone or in combination with another...

Part H— Pharmaceutical Distribution Supply Chain

§ 360eee. Definitions - (1) AffiliateThe term “affiliate” means a business entity that has...

§ 360eee–1. Requirements - (a) In general(1) Other activitiesEach manufacturer, repackager, wholesale distributor, and...

§ 360eee–2. National standards for prescription drug wholesale distributors - (a) In generalThe Secretary shall, not later than 2 years...

§ 360eee–3. National standards for third-party logistics providers - (a) RequirementsNo third-party logistics provider in any State may conduct...

§ 360eee–4. Uniform national policy - (a) Product tracing and other requirementsBeginning on November 27, 2013,...

Part I— Nonprescription Sunscreen and Other Active Ingredients

§ 360fff. Definitions - (1) the term “Advisory Committee” means the Nonprescription Drug Advisory...

§ 360fff–1. Submission of requests - Any person may submit a request to the Secretary for...

§ 360fff–2. Eligibility determinations; data submission; filing - (a) Eligibility determinations(1) In generalNot later than 60 calendar days...

§ 360fff–3. GRASE determination - (a) Review of new request(1) Proposed sunscreen orderIn the case...

§ 360fff–4. Guidance; other provisions - (a) Guidance(1) In general(A) Draft guidanceNot later than 1 year...

§ 360fff–5. Repealed. , , -

§ 360fff–6. Non-sunscreen time and extent applications - (a) Pending time and extent applications(1) In general(A) Request for...

§ 360fff–7. Report - (a) In general(1) In generalNot later than 18 months after...

§ 360fff–8. Sunset - This part shall cease to be effective at the end...

SUBCHAPTER VI— COSMETICS

§ 361. Adulterated cosmetics - (a) If it bears or contains any poisonous or deleterious...

§ 362. Misbranded cosmetics - (a) If its labeling is false or misleading in any...

§ 363. Regulations making exemptions - The Secretary shall promulgate regulations exempting from any labeling requirement...

§ 364. Definitions - (1) Adverse eventThe term “adverse event” means any health-related event...

§ 364a. Adverse events - (a) Serious adverse event reporting requirementsThe responsible person shall submit...

§ 364b. Good manufacturing practice - (a) In generalThe Secretary shall by regulation establish good manufacturing...

§ 364c. Registration and product listing - (a) Submission of registration(1) Initial registration(A) Existing facilitiesEvery person that,...

§ 364d. Safety substantiation - (a) Substantiation of safetyA responsible person for a cosmetic product...

§ 364e. Labeling - (a) General requirementEach cosmetic product shall bear a label that...

§ 364f. Records - (a) In generalIf the Secretary has a reasonable belief that...

§ 364g. Mandatory recall authority - (a) In generalIf the Secretary determines that there is a...

§ 364h. Small businesses - (a) In generalResponsible persons, and owners and operators of facilities,...

§ 364i. Exemption for certain products and facilities - (a) In generalNotwithstanding any other provision of law, except as...

§ 364j. Preemption - (a) In generalNo State or political subdivision of a State...

SUBCHAPTER VII— GENERAL AUTHORITY

Part A— General Administrative Provisions

§ 371. Regulations and hearings - (a) Authority to promulgate regulationsThe authority to promulgate regulations for...

§ 372. Examinations and investigations - (a) Authority to conduct(1)(A) The Secretary is authorized to conduct...

§ 372a. Transferred -

§ 373. Records - (a) In generalFor the purpose of enforcing the provisions of...

§ 374. Inspection - (a) Right of agents to enter; scope of inspection; notice;...

§ 374a. Inspections relating to food allergens - (1) to ensure that the entities operating the facilities comply...

§ 375. Publicity - (a) ReportsThe Secretary shall cause to be published from time...

§ 376. Examination of sea food on request of packer; marking food with results; fees; penalties - The Secretary, upon application of any packer of any sea...

§ 377. Revision of United States Pharmacopoeia; development of analysis and mechanical and physical tests - The Secretary, in carrying into effect the provisions of the...

§ 378. Advertising of foods - (a) Determination of misbranding; notification of Federal Trade Commission by...

§ 379. Confidential information - (a) ContractorsThe Secretary may provide any information which is exempt...

§ 379a. Presumption of existence of jurisdiction - In any action to enforce the requirements of this chapter...

§ 379b. Consolidated administrative and laboratory facility - (a) AuthorityThe Secretary, in consultation with the Administrator of the...

§ 379c. Transferred -

§ 379d. Automation of Food and Drug Administration - (a) In generalThe Secretary, acting through the Commissioner of Food...

§ 379d–1. Conflicts of interest - (a) DefinitionsFor purposes of this section:(1) Advisory committeeThe term “advisory...

§ 379d–2. Policy on the review and clearance of scientific articles published by FDA employees - (a) DefinitionIn this section, the term “article” means a paper,...

§ 379d–3. Streamlined hiring authority - (a) In generalIn addition to any other personnel authorities under...

§ 379d–3a. Hiring authority for scientific, technical, and professional personnel - (a) In generalThe Secretary may, notwithstanding title 5, governing appointments...

§ 379d–3b. Strategic Workforce Plan and report - (a) In generalNot later than September 30, 2023, and at...

§ 379d–4. Reporting requirements - (a) Generic drugsBeginning with fiscal year 2013 and ending after...

§ 379d–5. Guidance document regarding product promotion using the Internet - Not later than 2 years after , the Secretary of...

Part B— Colors

§ 379e. Listing and certification of color additives for foods, drugs, devices, and cosmetics - (a) Unsafe color additivesA color additive shall, with respect to...

Part C— Fees -

Part D— Information and Education

§ 379k. Information system - The Secretary shall establish and maintain an information system to...

§ 379k–1. Electronic format for submissions - (a) Drugs and biologics(1) In generalBeginning no earlier than 24...

§ 379l. Education - (a) In generalThe Secretary shall conduct training and education programs...

Part E— Environmental Impact Review

§ 379o. Environmental impact - Notwithstanding any other provision of law, an environmental impact statement...

Part F— National Uniformity for Nonprescription Drugs and Preemption for Labeling or Packaging of Cosmetics

§ 379r. National uniformity for nonprescription drugs - (a) In generalExcept as provided in subsection (b), (c)(1), (d),...

§ 379s. Preemption for labeling or packaging of cosmetics - (a) In generalExcept as provided in subsection (b), (d), or...

Part G— Safety Reports

§ 379v. Safety report disclaimers - With respect to any entity that submits or is required...

Part H— Serious Adverse Event Reports

§ 379aa. Serious adverse event reporting for nonprescription drugs - (a) DefinitionsIn this section:(1) Adverse eventThe term “adverse event” means...

§ 379aa–1. Serious adverse event reporting for dietary supplements - (a) DefinitionsIn this section:(1) Adverse eventThe term “adverse event” means...

Part I— Reagan-Udall Foundation for the Food and Drug Administration

§ 379dd. Establishment and functions of the Foundation - (a) In generalA nonprofit corporation to be known as the...

§ 379dd–1. Location of Foundation - The Foundation shall, if practicable, be located not more than...

§ 379dd–2. Activities of the Food and Drug Administration - (a) In generalThe Commissioner shall receive and assess the report...

SUBCHAPTER VIII— IMPORTS AND EXPORTS

§ 381. Imports and exports - (a) Imports; list of registered foreign establishments; samples from unregistered...

§ 382. Exports of certain unapproved products - (a) Drugs or devices intended for human or animal use...

§ 383. Office of International Relations - (a) EstablishmentThere is established in the Department of Health and...

§ 384. Importation of prescription drugs - (a) DefinitionsIn this section:(1) ImporterThe term “importer” means a pharmacist...

§ 384a. Foreign supplier verification program - (a) In general(1) Verification requirementExcept as provided under subsections (e)...

§ 384b. Voluntary qualified importer program - (a) In generalBeginning not later than 18 months after January...

§ 384c. Inspection of foreign food facilities - (a) InspectionThe Secretary—(1) may enter into arrangements and agreements with...

§ 384d. Accreditation of third-party auditors - (a) DefinitionsIn this section:(1) Audit agentThe term “audit agent” means...

§ 384e. Recognition of foreign government inspections - (a) InspectionThe Secretary—(1) may enter into arrangements and agreements with...

§ 384f. Strengthening FDA and CBP coordination and capacity - (a) In generalThe Secretary of Health and Human Services (referred...

§ 384g. Restricting entrance of illicit drugs - (a) Food and Drug Administration and U.S. Customs and Border...

SUBCHAPTER IX— TOBACCO PRODUCTS

§ 387. Definitions - (1) AdditiveThe term “additive” means any substance the intended use...

§ 387a. FDA authority over tobacco products - (a) In generalTobacco products, including modified risk tobacco products for...

§ 387a–1. Final rule - (a) Cigarettes and smokeless tobacco(1) In generalOn the first day...

§ 387b. Adulterated tobacco products - (1) it consists in whole or in part of any...

§ 387c. Misbranded tobacco products - (a) In generalA tobacco product shall be deemed to be...

§ 387d. Submission of health information to the Secretary - (a) RequirementEach tobacco product manufacturer or importer, or agents thereof,...

§ 387e. Annual registration - (a) DefinitionsIn this section:(1) Manufacture, preparation, compounding, or processingThe term...

§ 387f. General provisions respecting control of tobacco products - (a) In generalAny requirement established by or under section 387b,...

§ 387f–1. Enforcement action plan for advertising and promotion restrictions - (a) Action plan(1) DevelopmentNot later than 6 months after June...

§ 387g. Tobacco product standards - (a) In general(1) Special rules(A) Special rule for cigarettesBeginning 3...

§ 387h. Notification and other remedies - (a) NotificationIf the Secretary determines that—(1) a tobacco product which...

§ 387i. Records and reports on tobacco products - (a) In generalEvery person who is a tobacco product manufacturer...

§ 387j. Application for review of certain tobacco products - (a) In general(1) New tobacco product definedFor purposes of this...

§ 387k. Modified risk tobacco products - (a) In generalNo person may introduce or deliver for introduction...

§ 387l. Judicial review - (a) Right to review(1) In generalNot later than 30 days...

§ 387m. Equal treatment of retail outlets - The Secretary shall issue regulations to require that retail establishments...

§ 387n. Jurisdiction of and coordination with the Federal Trade Commission - (a) Jurisdiction(1) In generalExcept where expressly provided in this subchapter,...

§ 387o. Regulation requirement - (a) Testing, reporting, and disclosureNot later than 36 months after...

§ 387p. Preservation of State and local authority - (a) In general(1) PreservationExcept as provided in paragraph (2)(A), nothing...

§ 387q. Tobacco Products Scientific Advisory Committee - (a) EstablishmentNot later than 6 months after June 22, 2009,...

§ 387r. Drug products used to treat tobacco dependence - (a) In generalThe Secretary shall—(1) at the request of the...

§ 387s. User fees - (a) Establishment of quarterly feeBeginning on June 22, 2009, the...

§ 387t. Labeling, recordkeeping, records inspection - (a) Origin labeling(1) RequirementBeginning 1 year after June 22, 2009,...

§ 387u. Studies of progress and effectiveness - (a) FDA reportNot later than 3 years after June 22,...

§ 387v. Reporting on tobacco regulation activities - (a) In generalFor fiscal year 2022 and each subsequent fiscal...

SUBCHAPTER X— MISCELLANEOUS

§ 391. Separability clause - If any provision of this chapter is declared unconstitutional, or...

§ 392. Exemption of meats and meat food products - (a) Law determinative of exemptionMeats and meat food products shall...

§ 393. Food and Drug Administration - (a) In generalThere is established in the Department of Health...

§ 393a. Office of Pediatric Therapeutics - (a) EstablishmentThe Secretary of Health and Human Services shall establish...

§ 394. Scientific review groups - (1) establish such technical and scientific review groups as are...

§ 395. Loan repayment program - (a) In general(1) Authority for programSubject to paragraph (2), the...

§ 396. Practice of medicine - Nothing in this chapter shall be construed to limit or...

§ 397. Contracts for expert review - (a) In general(1) AuthorityThe Secretary may enter into a contract...

§ 398. Notices to States regarding imported food - (a) In generalIf the Secretary has credible evidence or information...

§ 399. Grants to enhance food safety - (a) In generalThe Secretary is authorized to make grants to...

§ 399a. Office of the Chief Scientist - (a) Establishment; appointmentThe Secretary shall establish within the Office of...

§ 399b. Office of Women’s Health - (a) EstablishmentThere is established within the Office of the Commissioner,...

§ 399c. Improving the training of State, local, territorial, and tribal food safety officials - (a) TrainingThe Secretary shall set standards and administer training and...

§ 399d. Employee protections - (a) In generalNo entity engaged in the manufacture, processing, packing,...

§ 399e. Nanotechnology - (a) In generalThe Secretary of Health and Human Services (referred...

§ 399f. Ensuring adequate information regarding pharmaceuticals for all populations, particularly underrepresented subpopulations, including racial subgroups - (a) Communication planThe Secretary of Health and Human Services (referred...

§ 399g. Food and Drug Administration Intercenter Institutes - (a) In generalThe Secretary shall establish one or more Intercenter...

§ 399h. National Centers of Excellence in Advanced and Continuous Pharmaceutical Manufacturing - (a) In generalThe Secretary of Health and Human Services, acting...

§ 399i. Food and Drug Administration Working Capital Fund - (a) In generalThere is hereby established in the Treasury of...

CHAPTER 10— POULTRY AND POULTRY PRODUCTS INSPECTION

§ 451. Congressional statement of findings - Poultry and poultry products are an important source of the...

§ 452. Congressional declaration of policy - It is hereby declared to be the policy of the...

§ 453. Definitions - (a) The term “commerce” means commerce between any State, any...

§ 454. Federal and State cooperation in development and administration of State poultry product inspection programs - (a) State laws; planning, technical and financial assistance; advisory committeesIt...

§ 455. Inspection in official establishments - (a) Ante mortem inspectionFor the purpose of preventing the entry...

§ 456. Operation of premises, facilities and equipment - (a) Sanitary practicesEach official establishment slaughtering poultry or processing poultry...

§ 457. Labeling and container standards - (a) Requirements for shipping containers and immediate containers; nonconsumer packaged...

§ 458. Prohibited acts - (a) No person shall—(1) slaughter any poultry or process any...

§ 459. Compliance by all establishments - (a) In generalNo establishment processing poultry or poultry products for...

§ 460. Miscellaneous activities subject to regulation - (a) Prohibition of inspection of articles not intended for use...

§ 461. Offenses and punishment - (a) Violations; liability of agents, employees, and employersAny person who...

§ 462. Reporting of violations; notice; opportunity to present views - Before any violation of this chapter is reported by the...

§ 463. Rules and regulations - (a) Storage and handling of poultry products; violation of regulationsThe...

§ 464. Exemptions - (a) Persons exemptedThe Secretary shall, by regulation and under such...

§ 465. Limitations upon entry of poultry products and other materials into official establishments - The Secretary may limit the entry of poultry products and...

§ 466. Imports - (a) Compliance with standards and regulations; status after importationNo slaughtered...

§ 467. Inspection services - (a) Refusal or withdrawal; hearing; business unfitness based upon certain...

§ 467a. Administrative detention; duration; pending judicial proceedings; notification of government authorities; release; removal of official marks - Whenever any poultry product, or any product exempted from the...

§ 467b. Seizure and condemnation - (a) Proceedings in rem; libel of information; jurisdiction; disposal by...

§ 467c. Federal court jurisdiction of enforcement and injunction proceedings and other kinds of cases; limitations; United States as plaintiff; subpenas - The United States district courts, the District Court of Guam,...

§ 467d. Administration and enforcement; applicability of penalty provisions; conduct of inquiries; power and jurisdiction of courts - For the efficient administration and enforcement of this chapter, the...

§ 467e. Non-Federal jurisdiction of federally regulated matters; prohibition of additional or different requirements for establishments with inspection services and as to marking, labeling, packaging, and ingredients; recordkeeping and related requirements; concurrent jurisdiction over distribution for human food purposes of adulterated or misbranded and imported articles; other matters - Requirements within the scope of this chapter with respect to...

§ 467f. Federal Food, Drug, and Cosmetic Act applications - (a) Exemptions; authorities under food, drug, and cosmetic provisions unaffectedPoultry...

§ 468. Cost of inspection; overtime - The cost of inspection rendered under the requirements of this...

§ 469. Authorization of appropriations - There is authorized to be appropriated such sums as are...

§ 470. Omitted -

§ 471. Safe Meat and Poultry Inspection Panel - (a) Review and evaluationThe advisory panel known as the “Safe...

§ 472. Interstate shipment of poultry inspected by Federal and State agencies for certain small establishments - (a) Definitions(1) Appropriate State agencyThe term “appropriate State agency” means...

§ 473. Grants for improvements to meat and poultry facilities to allow for interstate shipment - (a) In generalThe Secretary shall make grants to meat and...

CHAPTER 11— MANUFACTURE OF NARCOTIC DRUGS

§§ 501 to 517. Repealed. , , -

CHAPTER 12— MEAT INSPECTION

SUBCHAPTER I— INSPECTION REQUIREMENTS; ADULTERATION AND MISBRANDING

§ 601. Definitions - (a) The term “Secretary” means the Secretary of Agriculture of...

§ 602. Congressional statement of findings - Meat and meat food products are an important source of...

§ 603. Examination of animals prior to slaughter; use of humane methods - (a) Examination of animals before slaughtering; diseased animals slaughtered separately...

§ 604. Post mortem examination of carcasses and marking or labeling; destruction of carcasses condemned; reinspection - For the purposes hereinbefore set forth the Secretary shall cause...

§ 605. Examination of carcasses brought into slaughtering or packing establishments, and of meat food products issued from and returned thereto; conditions for entry - The foregoing provisions shall apply to all carcasses or parts...

§ 606. Inspection and labeling of meat food products - (a) In generalFor the purposes hereinbefore set forth the Secretary...

§ 607. Labeling, marking, and container requirements - (a) Labeling receptacles or coverings of meat or meat food...

§ 608. Sanitary inspection and regulation of slaughtering and packing establishments; rejection of adulterated meat or meat food products - The Secretary shall cause to be made, by experts in...

§ 609. Examination of animals and food products thereof, slaughtered and prepared during nighttime - The Secretary shall cause an examination and inspection of all...

§ 610. Prohibited acts - (a) Slaughtering animals or preparation of articles capable of use...

§ 611. Devices, marks, labels, and certificates; simulations - (a) Devices to be made under authorization of SecretaryNo brand...

§ 612. Notification - Any establishment subject to inspection under this chapter that believes,...

§ 613. Plans and reassessments - (1) prepare and maintain current procedures for the recall of...

§ 614. Repealed. , , -

§ 615. Inspection of carcasses, meat of which is intended for export - The Secretary shall also cause to be made a careful...

§ 616. Inspectors of carcasses, etc., meat of which is intended for export; certificates of condition - For the purpose of the Secretary may appoint inspectors who...

§ 617. Clearance prohibited to vessel carrying meat for export without inspector’s certificate - No clearance shall be given to any vessel having on...

§ 618. Delivery of inspectors’ certificates, and of copies - The inspectors provided for under this subchapter shall be authorized...

§ 619. Marking, labeling, or other identification to show kinds of animals from which derived; separate establishments for preparation and slaughtering activities - No person, firm, or corporation shall sell, transport, offer for...

§ 620. Imports - (a) Adulteration or misbranding prohibition; compliance with inspection, building construction...

§ 621. Inspectors to make examinations provided for; appointment; duties; regulations - The Secretary shall appoint from time to time inspectors to...

§ 622. Bribery of or gifts to inspectors or other officers and acceptance of gifts - Any person, firm, or corporation, or any agent or employee...

§ 623. Exemptions from inspection requirements - (a) Personal slaughtering and custom slaughtering for personal, household, guest,...

§ 624. Storage and handling regulations; violations; exemption of establishments subject to non-Federal jurisdiction - The Secretary may by regulations prescribe conditions under which carcasses,...

§ 625. Inapplicability of certain requirements to catfish - Notwithstanding any other provision of this chapter, the requirements of...

§ 626. Purchase of tags, labels, stamps, and certificates - The Secretary of Agriculture is authorized to expend appropriations for...

SUBCHAPTER II— MEAT PROCESSORS AND RELATED INDUSTRIES

§ 641. Prohibition of subchapter I inspection of articles not intended for use as human food; denaturation or other identification prior to distribution in commerce; inedible articles - Inspection shall not be provided under subchapter I of this...

§ 642. Recordkeeping requirements - (a) Classes of persons bound; scope of disclosure; access to...

§ 643. Registration of business, name of person, and trade names - No person, firm, or corporation shall engage in business, in...

§ 644. Regulation of transactions, transportation, or importation of 4–D animals to prevent use as human food - No person, firm, or corporation engaged in the business of...

§ 645. Federal provisions applicable to State or Territorial business transactions of a local nature and not subject to local authority - The authority conferred on the Secretary by section 642, 643,...

SUBCHAPTER III— FEDERAL AND STATE COOPERATION

§ 661. Federal and State cooperation - (a) Congressional statement of policyIt is the policy of the...

SUBCHAPTER IV— AUXILIARY PROVISIONS

§ 671. Inspection services; refusal or withdrawal; hearing; business unfitness based upon certain convictions; other provisions for withdrawal of services unaffected; responsible connection with business; finality of Secretary’s actions; judicial review; record - The Secretary may (for such period, or indefinitely, as he...

§ 672. Administrative detention; duration; pending judicial proceedings; notification of governmental authorities; release - Whenever any carcass, part of a carcass, meat or meat...

§ 673. Seizure and condemnation - (a) Proceedings in rem; libel of information; jurisdiction; disposal by...

§ 674. Federal court jurisdiction of enforcement and injunction proceedings and other kinds of cases; limitations of - The United States district courts, the District Court of Guam,...

§ 675. Assaulting, resisting, or impeding certain persons; murder; protection of such persons - Any person who forcibly assaults, resists, opposes, impedes, intimidates, or...

§ 676. Violations - (a) Misdemeanors; felonies: intent to defraud and distribution of adulterated...

§ 677. Other Federal laws applicable for administration and enforcement of chapter; location of inquiries; jurisdiction of Federal courts - For the efficient administration and enforcement of this chapter, the...

§ 678. Non-Federal jurisdiction of federally regulated matters; prohibition of additional or different requirements for establishments with inspection services and as to marking, labeling, packaging, and ingredients; recordkeeping and related requirements; concurrent jurisdiction over distribution for human food purposes of adulterated or misbranded and imported articles; other matters - Requirements within the scope of this chapter with respect to...

§ 679. Application of Federal Food, Drug, and Cosmetic Act - (a) Authorities under food, drug, and cosmetic provisions unaffectedNotwithstanding any...

§ 679a. Safe Meat and Poultry Inspection Panel - (a) EstablishmentThere is established in the Department of Agriculture a...

§ 679b. Pasteurization of meat and poultry - (1) In generalEffective beginning not later than 30 days after...

§ 679c. Expansion of Food Safety Inspection Service activities - (a) In generalThe Secretary of Agriculture may utilize existing authorities...

§ 680. Authorization of appropriations - There are hereby authorized to be appropriated such sums as...

SUBCHAPTER IV–A— INSPECTIONS BY FEDERAL AND STATE AGENCIES

§ 683. Interstate shipment of meat inspected by Federal and State agencies for certain small establishments - (a) Definitions(1) Appropriate State agencyThe term “appropriate State agency” means...

SUBCHAPTER V— MISCELLANEOUS PROVISIONS

§ 691. Omitted -

§ 692. Inspection extended to reindeer - The provisions of the meat-inspection law may be extended to...

§ 693. Inspection of dairy products for export - The act of , as amended, for the inspection of...

§ 694. Authorization of appropriations - Annual appropriations of the sum of $3,000,000 from the general...

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US Code Title 21— FOOD AND DRUGS

US Code
Title 21— FOOD AND DRUGS