Regulations.gov document
Reference 3 - FDA. Questions and Answers Regarding Adverse Event Reporting and…
Supporting & Related Material · FDA-2010-D-0605 · posted Dec 16, 2010
Key facts
| Document ID | FDA-2010-D-0605-0005 |
|---|---|
| Title | Reference 3 - FDA. Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act, http://www.fda.gov/FoodGuidances |
| Document type | Supporting & Related Material |
| Subtype | GDL-Guidance |
| Agency | FDA |
| Docket | FDA-2010-D-0605 |
| Posted | Dec 16, 2010 |
At a glance
- 1–9 Public comments on this docket
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