FDA Inspection
Peter S. Hersh, M.D.Peter S. Hersh, M.D. – FDA Inspection, Mar 9, 2012
Record Details
This FDA Inspection record concerns Peter S. Hersh, M.D., with an inspection on March 9, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Peter S. Hersh, M.D.
- Inspection Date
- March 9, 2012
- Product Type
- Devices
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ID · 590898f5-a5af-4a9f-9a49-2e7639353fa6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 773531
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 812.140(a)(3)(ii)Investigator adverse effect records inadequate
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
- 21 CFR 812.140(a)(1)Investigator correspondence records inadequate
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Other FDA inspections of Peter S. Hersh, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 16, 2014 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Peter S. Hersh, M.D.
- FDA Inspection 864023 - 2014-01-16
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