Code of Federal Regulations · Subpart

Subpart S — Additional Traceability Records For Certain Foods

21 C.F.R. pt. 1, subpt. S

• § 1.1300 Who Is Subject To This Subpart?
• § 1.1305 What Foods And Persons Are Exempt From This Subpart?
• § 1.1310 What Definitions Apply To This Subpart?
• § 1.1315 What Traceability Plan Must I Have For Foods On The Food Traceability List That I Manufacture, Process, Pack, Or Hold?
• § 1.1320 When Must I Assign Traceability Lot Codes To Foods On The Food Traceability List?
• § 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?
• § 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?
• § 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?
• § 1.1455 How Must Records Required By This Subpart Be Maintained And Made Available?
• § 1.1460 What Consequences Could Result From Failing To Comply With The Requirements Of This Subpart?
• § 1.1465 How Will Fda Update The Food Traceability List?