Federal (United States) · Regulations
Subpart S — Additional Traceability Records for Certain Foods
33 sections
33 sections
- 21 C.F.R. § 1.1300Who is subject to this subpart?
- 21 C.F.R. § 1.1305What foods and persons are exempt from this subpart?
- 21 C.F.R. § 1.1310What definitions apply to this subpart?
- 21 C.F.R. § 1.1315What traceability plan must I have for foods on the Food Traceability List that I manufacture, process, pack, or hold?
- 21 C.F.R. § 1.1320When must I assign traceability lot codes to foods on the Food Traceability List?
- 21 C.F.R. § 1.1325What records must I keep and provide when I harvest or cool a raw agricultural commodity on the Food Traceability List?
- 21 C.F.R. § 1.1330What records must I keep when I am performing the initial packing of a raw agricultural commodity (other than a food obtained from a fishing vessel) on the Food Traceability List?
- 21 C.F.R. § 1.1335What records must I keep when I am the first land-based receiver of a food on the Food Traceability List that was obtained from a fishing vessel?
- 21 C.F.R. § 1.1340What records must I keep and provide when I ship a food on the Food Traceability List?
- 21 C.F.R. § 1.1345What records must I keep when I receive a food on the Food Traceability List?
- 21 C.F.R. § 1.1350What records must I keep when I transform a food on the Food Traceability List?
- 21 C.F.R. § 1.1360Under what circumstances will FDA modify the requirements in this subpart that apply to a food or type of entity or exempt a food or type of entity from the requirements of this subpart?
- 21 C.F.R. § 1.1365When will FDA consider whether to adopt modified requirements or grant an exemption from the requirements of this subpart?
- 21 C.F.R. § 1.1370What must be included in a petition requesting modified requirements or an exemption from the requirements?
- 21 C.F.R. § 1.1375What information submitted in a petition requesting modified requirements or an exemption, or information in comments on such a petition, is publicly available?
- 21 C.F.R. § 1.1380What process applies to a petition requesting modified requirements or an exemption?
- 21 C.F.R. § 1.1385What process will FDA follow when adopting modified requirements or granting an exemption on our own initiative?
- 21 C.F.R. § 1.1390When will modified requirements that we adopt or an exemption that we grant become effective?
- 21 C.F.R. § 1.1395Under what circumstances may FDA revise or revoke modified requirements or an exemption?
- 21 C.F.R. § 1.1400What procedures apply if FDA tentatively determines that modified requirements or an exemption should be revised or revoked?
- 21 C.F.R. § 1.1405Under what circumstances will FDA waive one or more of the requirements of this subpart for an individual entity or a type of entity?
- 21 C.F.R. § 1.1410When will FDA consider whether to waive a requirement of this subpart?
- 21 C.F.R. § 1.1415How may I request a waiver for an individual entity?
- 21 C.F.R. § 1.1420What process applies to a request for a waiver for an individual entity?
- 21 C.F.R. § 1.1425What must be included in a petition requesting a waiver for a type of entity?
- 21 C.F.R. § 1.1430What information submitted in a petition requesting a waiver for a type of entity, or information in comments on such a petition, is publicly available?
- 21 C.F.R. § 1.1435What process applies to a petition requesting a waiver for a type of entity?
- 21 C.F.R. § 1.1440What process will FDA follow when waiving a requirement of this subpart on our own initiative?
- 21 C.F.R. § 1.1445Under what circumstances may FDA modify or revoke a waiver?
- 21 C.F.R. § 1.1450What procedures apply if FDA tentatively determines that a waiver should be modified or revoked?
- 21 C.F.R. § 1.1455How must records required by this subpart be maintained and made available?
- 21 C.F.R. § 1.1460What consequences could result from failing to comply with the requirements of this subpart?
- 21 C.F.R. § 1.1465How will FDA update the Food Traceability List?