Code of Federal Regulations (Last Updated: May 6, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter B - Food for Human Consumption |
Part 111 - Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements |
Subpart O - Product Complaints |
§ 111.553 - What are the requirements under this subpart O for written procedures? |
§ 111.560 - What requirements apply to the review and investigation of a product complaint? |
§ 111.570 - Under this subpart O, what records must you make and keep? |