{"data":{"id":"us/21-cfr-111.525","jurisdiction":"us","citation":"21 CFR 111.525","heading":"What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing?","body":"(a) You must ensure that any returned dietary supplements that are reprocessed meet all product specifications established in accordance with § 111.70(e); and\n(b) Quality control personnel must approve or reject the release for distribution of any returned dietary supplement that is reprocessed.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION","PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS","Subpart N—Returned Dietary Supplements"],"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":"4941c40ef2a6d0ee038b13cd27c827d0b25961d696def2003955571d37e3b434","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-111.520","next":"us/21-cfr-111.530"},"notice":"GroundRules: Original legal text. Not legal advice."}