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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 N - Returned Dietary Supplements |
| § 111.503 - What are the requirements under this subpart N for written procedures? |
| § 111.510 - What requirements apply when a returned dietary supplement is received? |
| § 111.515 - When must a returned dietary supplement be destroyed, or otherwise suitably disposed of? |
| § 111.520 - When may a returned dietary supplement be salvaged? |
| § 111.525 - What requirements apply to a returned dietary supplement that quality control personnel approve for reprocessing? |
| § 111.530 - When must an investigation be conducted of your manufacturing processes and other batches? |
| § 111.535 - Under this subpart N, what records must you make and keep? |