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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 D - Equipment and Utensils |
| § 111.25 - What are the requirements under this subpart D for written procedures? |
| § 111.27 - What requirements apply to the equipment and utensils that you use? |
| § 111.30 - What requirements apply to automated, mechanical, or electronic equipment? |
| § 111.35 - Under this subpart D, what records must you make and keep? |