SUBPART F—Production and Process Control System: Requirements for Quality Control (§111.103 to §111.140)
- 111.103—What are the requirements under this subpart F for written procedures?
- 111.105—What must quality control personnel do?
- 111.110—What quality control operations are required for laboratory operations associated with the production and process control system?
- 111.113—What quality control operations are required for a material review and disposition decision?
- 111.117—What quality control operations are required for equipment, instruments, and controls?
- 111.120—What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?
- 111.123—What quality control operations are required for the master manufacturing record, the batch production record, and manufacturing operations?
- 111.127—What quality control operations are required for packaging and labeling operations?
- 111.130—What quality control operations are required for returned dietary supplements?
- 111.135—What quality control operations are required for product complaints?
- 111.140—Under this subpart F, what records must you make and keep?