21 CFR Subpart S - Subpart S—Additional Traceability Records for Certain Foods
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General Provisions (§§ 1.1300 - 1.1310)
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Records of Critical Tracking Events (§§ 1.1325 - 1.1350)
- § 1.1325 What records must I keep and provide when I harvest or cool a raw agricultural commodity on the Food Traceability List?
- § 1.1330 What 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?
- § 1.1335 What 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?
- § 1.1340 What records must I keep and provide when I ship a food on the Food Traceability List?
- § 1.1345 What records must I keep when I receive a food on the Food Traceability List?
- § 1.1350 What records must I keep when I transform a food on the Food Traceability List?
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Procedures for Modified Requirements and Exemptions (§§ 1.1360 - 1.1400)
- § 1.1360 Under 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?
- § 1.1365 When will FDA consider whether to adopt modified requirements or grant an exemption from the requirements of this subpart?
- § 1.1370 What must be included in a petition requesting modified requirements or an exemption from the requirements?
- § 1.1375 What information submitted in a petition requesting modified requirements or an exemption, or information in comments on such a petition, is publicly available?
- § 1.1380 What process applies to a petition requesting modified requirements or an exemption?
- § 1.1385 What process will FDA follow when adopting modified requirements or granting an exemption on our own initiative?
- § 1.1390 When will modified requirements that we adopt or an exemption that we grant become effective?
- § 1.1395 Under what circumstances may FDA revise or revoke modified requirements or an exemption?
- § 1.1400 What procedures apply if FDA tentatively determines that modified requirements or an exemption should be revised or revoked?
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Waivers (§§ 1.1405 - 1.1450)
- § 1.1405 Under what circumstances will FDA waive one or more of the requirements of this subpart for an individual entity or a type of entity?
- § 1.1410 When will FDA consider whether to waive a requirement of this subpart?
- § 1.1415 How may I request a waiver for an individual entity?
- § 1.1420 What process applies to a request for a waiver for an individual entity?
- § 1.1425 What must be included in a petition requesting a waiver for a type of entity?
- § 1.1430 What information submitted in a petition requesting a waiver for a type of entity, or information in comments on such a petition, is publicly available?
- § 1.1435 What process applies to a petition requesting a waiver for a type of entity?
- § 1.1440 What process will FDA follow when waiving a requirement of this subpart on our own initiative?
- § 1.1445 Under what circumstances may FDA modify or revoke a waiver?
- § 1.1450 What procedures apply if FDA tentatively determines that a waiver should be modified or revoked?
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Records Maintenance and Availability (§ 1.1455)
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Consequences of Failure To Comply (§ 1.1460)
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Updating the Food Traceability List (§ 1.1465)
Source:
87 FR 71077, Nov. 21, 2022, unless otherwise noted.