FDA Inspection
Cohen Kenneth, MDCohen Kenneth, MD – FDA Inspection, Jul 29, 2009
Record Details
This FDA Inspection record concerns Cohen Kenneth, MD, with an inspection on July 29, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Cohen Kenneth, MD
- Inspection Date
- July 29, 2009
- Product Type
- Biologics
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ID · 2b731ae9-3993-42b0-b537-6367ea55daff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 601960
- FDA center
- Biologics
- 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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