FDA Inspection
Robert C. G. Martin, II, M.D., PhD.Robert C. G. Martin, II, M.D., PhD. – FDA Inspection, Jan 25, 2017
Record Details
This FDA Inspection record concerns Robert C. G. Martin, II, M.D., PhD., with an inspection on January 25, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · dc006ed9-d492-43e6-a0fb-20f220b05da7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 998393
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.100Investigator lack of control of investigational devices
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Robert C. G. Martin, II, M.D., PhD.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| December 3, 2010 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Robert C. G. Martin, II, M.D., PhD.
- FDA Inspection 701939 - 2010-12-03
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