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Table of Contents

Chapter I: FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

Subchapter A: General


Part 1: General enforcement regulations


Subpart I: Prior notice of imported food


21 CFR 1.277 - What is the scope of this subpart?

21 CFR 1.278 - Who is authorized to submit prior notice?

21 CFR 1.279 - When must prior notice be submitted to FDA?

21 CFR 1.280 - How must you submit prior notice?

21 CFR 1.281 - What information must be in a prior notice?

21 CFR 1.282 - What must you do if information changes after you have received confirmation of a prior notice from FDA?

21 CFR 1.283 - What happens to food that is imported or offered for import without adequate prior notice?

21 CFR 1.284 - What are the other consequences of failing to submit adequate prior notice or otherwise failing to comply with this subpart?

21 CFR 1.285 - What happens to food that is imported or offered for import from unregistered facilities that are required to register under 21 CFR part 1, subpart H?

Subpart J: Establishment, maintenance, and availability of records


21 CFR 1.326 - Who is subject to this subpart?

21 CFR 1.327 - Who is excluded from all or part of the regulations in this subpart?

21 CFR 1.328 - What definitions apply to this subpart?

21 CFR 1.329 - Do other statutory provisions and regulations apply?

21 CFR 1.330 - Can existing records satisfy the requirements of this subpart?

21 CFR 1.337 - What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate previous sources of food?

21 CFR 1.345 - What information must nontransporters establish and maintain to identify the nontransporter and transporter immediate subsequent recipients of food?

21 CFR 1.352 - What information must transporters establish and maintain?

21 CFR 1.360 - What are the record retention requirements?

21 CFR 1.361 - What are the record availability requirements?

21 CFR 1.362 - What records are excluded from this subpart?

21 CFR 1.363 - What are the consequences of failing to establish or maintain records or make them available to FDA as required by this subpart?

21 CFR 1.368 - What are the compliance dates for this subpart?

Subpart K: Administrative detention of food for human or animal consumption


21 CFR 1.377 - What definitions apply to this subpart?

21 CFR 1.378 - What criteria does FDA use to order a detention?

21 CFR 1.379 - How long may FDA detain an article of food?

21 CFR 1.380 - Where and under what conditions must the detained article of food be held?

21 CFR 1.381 - May a detained article of food be delivered to another entity or transferred to another location?

21 CFR 1.382 - What labeling or marking requirements apply to a detained article of food?

21 CFR 1.383 - What expedited procedures apply when FDA initiates a seizure action against a detained perishable food?

21 CFR 1.384 - When does a detention order terminate?