FDA Inspection
James N. Moy, M.D.James N. Moy, M.D. – FDA Inspection, Jun 16, 2009
Record Details
This FDA Inspection record concerns James N. Moy, M.D., with an inspection on June 16, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- James N. Moy, M.D.
- Inspection Date
- June 16, 2009
- Product Type
- Biologics
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ID · ae035b9b-6c8f-4ea1-bbd9-5cec102767d0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 589005
- FDA center
- Biologics
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 312.50Ensuring compliance with plan and protocol
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
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Other FDA inspections of James N. Moy, M.D.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 30, 2015 | VAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
| May 22, 2009 | VAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
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