Part 111 — Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
- Subpt. A General Provisions §§111.1 to 111.5
- Subpt. B Personnel §§111.8 to 111.14
- Subpt. C Physical Plant and Grounds §§111.15 to 111.23
- Subpt. D Equipment and Utensils §§111.25 to 111.35
- Subpt. E Requirement to Establish a Production and Process Control System §§111.55 to 111.95
- Subpt. F Production and Process Control System: Requirements for Quality Control §§111.103 to 111.140
- Subpt. 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 §§111.153 to 111.180
- Subpt. H Production and Process Control System: Requirements for the Master Manufacturing Record §§111.205 to 111.210
- Subpt. I Production and Process Control System: Requirements for the Batch Production Record §§111.255 to 111.260
- Subpt. J Production and Process Control System: Requirements for Laboratory Operations §§111.303 to 111.325
- Subpt. K Production and Process Control System: Requirements for Manufacturing Operations §§111.353 to 111.375
- Subpt. L Production and Process Control System: Requirements for Packaging and Labeling Operations §§111.403 to 111.430
- Subpt. M Holding and Distributing §§111.453 to 111.475
- Subpt. N Returned Dietary Supplements §§111.503 to 111.535
- Subpt. O Product Complaints §§111.553 to 111.570
- Subpt. P Records and Recordkeeping §§111.605 to 111.610