{"data":{"id":"us/21-cfr-111.130","jurisdiction":"us","citation":"21 CFR 111.130","heading":"What quality control operations are required for returned dietary supplements?","body":"Quality control operations for returned dietary supplements must include:\n(a) Conducting any required material review and making any required disposition decision; including:\n(1) Determining whether tests or examination are necessary to determine compliance with product specifications established in accordance with § 111.70(e); and\n(2) Reviewing the results of any tests or examinations that are conducted to determine compliance with product specifications established in accordance with § 111.70(e);\n(b) Approving or rejecting any salvage and redistribution of any returned dietary supplement;\n(c) Approving or rejecting any reprocessing of any returned dietary supplement; and\n(d) Determining whether the reprocessed dietary supplement meets product specifications and either approving for release, or rejecting, 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 F—Production and Process Control System: Requirements for Quality Control"],"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":"90f848776fd2e28bf2832e48f9acc0bc240ba54b44b452a90a9b8776145e0d22","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-111.127","next":"us/21-cfr-111.135"},"notice":"GroundRules: Original legal text. Not legal advice."}