{"data":{"id":"us/21-cfr-111.120","jurisdiction":"us","citation":"21 CFR 111.120","heading":"What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?","body":"Quality control operations for components, packaging, and labels before use in the manufacture of a dietary supplement must include:\n(a) Reviewing all receiving records for components, packaging, and labels;\n(b) Determining whether all components, packaging, and labels conform to specifications established under § 111.70 (b) and (d);\n(c) Conducting any required material review and making any required disposition decision;\n(d) Approving or rejecting any treatment and in-process adjustments of components, packaging, or labels to make them suitable for use in the manufacture of a dietary supplement; and\n(e) Approving, and releasing from quarantine, all components, packaging, and labels before they are used.","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":"4185447199ed1a0ef6b012b997d578b866920856d3854d515eaec4123cf639a5","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-111.117","next":"us/21-cfr-111.123"},"notice":"GroundRules: Original legal text. Not legal advice."}