{"data":{"id":"us/21-cfr-1.1410","jurisdiction":"us","citation":"21 CFR 1.1410","heading":"When will FDA consider whether to waive a requirement of this subpart?","body":"FDA will consider whether to waive a requirement of this subpart on our own initiative or in response to the following:\n(a) A written request for a waiver for an individual entity; or\n(b) A citizen petition requesting a waiver for a type of entity submitted under § 10.30 of this chapter by any person subject to the requirements of this subpart.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER A—GENERAL","PART 1—GENERAL ENFORCEMENT REGULATIONS","Subpart S—Additional Traceability Records for Certain Foods"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"f1ab85189b992a07e0bd61e2d7079e7474acedfb1a0242d7f5ebfe73c7170a36","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-1.1405","next":"us/21-cfr-1.1415"},"notice":"GroundRules: Original legal text. Not legal advice."}