FDA Inspection
Roger S. Gammon, MDRoger S. Gammon, MD – FDA Inspection, Nov 8, 2010
Record Details
This FDA Inspection record concerns Roger S. Gammon, MD, with an inspection on November 8, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Roger S. Gammon, MD
- Inspection Date
- November 8, 2010
- Product Type
- Devices
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ID · c6f0c2eb-6585-41e9-923e-3ff1036f687c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 697176
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)(i)Investigator records of informed consent inadequate
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Other FDA inspections of Roger S. Gammon, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 30, 2012 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Roger S. Gammon, MD
- FDA Inspection 806274 - 2012-10-30
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