FDA Inspection
Goldman, Mitchel P MDGoldman, Mitchel P MD – FDA Inspection, Jun 12, 2009
Record Details
This FDA Inspection record concerns Goldman, Mitchel P MD, with an inspection on June 12, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Goldman, Mitchel P MD
- Inspection Date
- June 12, 2009
- Product Type
- Devices
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ID · f3cb53f8-06a1-45e1-abf6-bd3eb50ee1d0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 589023
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of Goldman, Mitchel P MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 24, 2012 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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