Part 111. PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS

• SUBPART A [§ 111.1 - § 111.5] - Subpart A—General Provisions
• SUBPART B [§ 111.8 - § 111.14] - Subpart B—Personnel
• SUBPART C [§ 111.15 - § 111.23] - Subpart C—Physical Plant and Grounds
• SUBPART D [§ 111.25 - § 111.35] - Subpart D—Equipment and Utensils
• SUBPART E [§ 111.55 - § 111.95] - Subpart E—Requirement to Establish a Production and Process Control System
• SUBPART F [§ 111.103 - § 111.140] - Subpart F—Production and Process Control System: Requirements for Quality Control
• SUBPART G [§ 111.153 - § 111.180] - 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
• SUBPART H [§ 111.205 - § 111.210] - Subpart H—Production and Process Control System: Requirements for the Master Manufacturing Record
• SUBPART I [§ 111.255 - § 111.260] - Subpart I—Production and Process Control System: Requirements for the Batch Production Record
• SUBPART J [§ 111.303 - § 111.325] - Subpart J—Production and Process Control System: Requirements for Laboratory Operations
• SUBPART K [§ 111.353 - § 111.375] - Subpart K—Production and Process Control System: Requirements for Manufacturing Operations
• SUBPART L [§ 111.403 - § 111.430] - Subpart L—Production and Process Control System: Requirements for Packaging and Labeling Operations
• SUBPART M [§ 111.453 - § 111.475] - Subpart M—Holding and Distributing
• SUBPART N [§ 111.503 - § 111.535] - Subpart N—Returned Dietary Supplements
• SUBPART O [§ 111.553 - § 111.570] - Subpart O—Product Complaints
• SUBPART P [§ 111.605 - § 111.610] - Subpart P—Records and Recordkeeping