FDA Inspection
Heidi J. Crayton, MDHeidi J. Crayton, MD – FDA Inspection, Jan 22, 2010
Record Details
This FDA Inspection record concerns Heidi J. Crayton, MD, with an inspection on January 22, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Heidi J. Crayton, MD
- Inspection Date
- January 22, 2010
- Product Type
- Drugs
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ID · 34ccfc71-6c8a-4e3c-b619-f614691b421c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 645901
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
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Other FDA inspections of Heidi J. Crayton, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 19, 2010 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Heidi J. Crayton, MD
- FDA Inspection 664742 - 2010-05-19
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