PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
- SUBPART A—General Provisions (§111.1 to §111.5)
- SUBPART B—Personnel (§111.8 to §111.14)
- SUBPART C—Physical Plant and Grounds (§111.15 to §111.23)
- SUBPART D—Equipment and Utensils (§111.25 to §111.35)
- SUBPART E—Requirement to Establish a Production and Process Control System (§111.55 to §111.95)
- SUBPART F—Production and Process Control System: Requirements for Quality Control (§111.103 to §111.140)
- SUBPART G—Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement (§111
- SUBPART H—Production and Process Control System: Requirements for the Master Manufacturing Record (§111.205 to §111.210)
- SUBPART I—Production and Process Control System: Requirements for the Batch Production Record (§111.255 to §111.260)
- SUBPART J—Production and Process Control System: Requirements for Laboratory Operations (§111.303 to §111.325)
- SUBPART K—Production and Process Control System: Requirements for Manufacturing Operations (§111.353 to §111.375)
- SUBPART L—Production and Process Control System: Requirements for Packaging and Labeling Operations (§111.403 to §111.430)
- SUBPART M—Holding and Distributing (§111.453 to §111.475)
- SUBPART N—Returned Dietary Supplements (§111.503 to §111.535)
- SUBPART O—Product Complaints (§111.553 to §111.570)
- SUBPART P—Records and Recordkeeping (§111.605 to §111.610)