FDA Inspection
George E Woodman M DGeorge E Woodman M D – FDA Inspection, Aug 14, 2014
Record Details
This FDA Inspection record concerns George E Woodman M D, with an inspection on August 14, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- George E Woodman M D
- Inspection Date
- August 14, 2014
- Product Type
- Devices
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ID · d62c3608-38ae-4d0c-aca6-841a78b3c8fa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 891483
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
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Other FDA inspections of George E Woodman M D
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 26, 2018 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 15, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for George E Woodman M D
- FDA Inspection 1071207 - 2018-10-26
- FDA Inspection 675795 - 2010-07-15
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