Site Feedback

Title 21

Displaying title 21, up to date as of 9/21/2021. Title 21 was last amended 9/21/2021.
eCFR Content

The Code of Federal Regulations (CFR) is the official legal print publication containing the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government. The Electronic Code of Federal Regulations (eCFR) is a continuously updated online version of the CFR. It is not an official legal edition of the CFR.

Learn more about the eCFR, its status, and the editorial process.

Title 21 Food and Drugs Part / Section
Chapter I Food and Drug Administration, Department of Health and Human Services 1 – 1299
Subchapter A General 1 – 99
Part 1 General Enforcement Regulations 1.1 – 1.980
Subpart J Establishment, Maintenance, and Availability of Records 1.326 – 1.368
General Provisions 1.326 – 1.330
§ 1.326 Who is subject to this subpart?
§ 1.327 Who is excluded from all or part of the regulations in this subpart?
§ 1.328 What definitions apply to this subpart?
§ 1.329 Do other statutory provisions and regulations apply?
§ 1.330 Can existing records satisfy the requirements of this subpart?
Requirements for Nontransporters To Establish and Maintain Records To Identify the Nontransporter and Transporter Immediate Previous Sources of Food 1.337
§ 1.337 What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate previous sources of food?
Requirements for Nontransporters To Establish and Maintain Records To Identify the Nontransporter and Transporter Immediate Subsequent Recipients of Food 1.345
§ 1.345 What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate subsequent recipients of food?
Requirements for Transporters To Establish and Maintain Records 1.352
§ 1.352 What information must transporters establish and maintain?
General Requirements 1.360 – 1.363
§ 1.360 What are the record retention requirements?
§ 1.361 What are the record availability requirements?
§ 1.362 What records are excluded from this subpart?
§ 1.363 What are the consequences of failing to establish or maintain records or make them available to FDA as required by this subpart?
Compliance Dates 1.368
§ 1.368 What are the compliance dates for this subpart?