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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter B - Food for Human Consumption |
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Part 111 - Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements |
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Subpart K - Production and Process Control System: Requirements for Manufacturing Operations |
| § 111.353 - What are the requirements under this subpart K for written procedures? |
| § 111.355 - What are the design requirements for manufacturing operations? |
| § 111.360 - What are the requirements for sanitation? |
| § 111.365 - What precautions must you take to prevent contamination? |
| § 111.370 - What requirements apply to rejected dietary supplements? |
| § 111.375 - Under this subpart K, what records must you make and keep? |