{"data":{"id":"us/21-cfr-117.320","jurisdiction":"us","citation":"21 CFR 117.320","heading":"Requirements for official review.","body":"All records required by this part must be made promptly available to a duly authorized representative of the Secretary of Health and Human Services for official review and copying upon oral or written request.","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 117—CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR HUMAN FOOD","Subpart F—Requirements Applying to Records That Must Be Established and Maintained"],"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":"ee90eea73dbced0ae03a149d8673d1e5d907cd10c1241801edebe7f45b79fe85","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-117.315","next":"us/21-cfr-117.325"},"notice":"GroundRules: Original legal text. Not legal advice."}