FDA Inspection
Gregory T. Simonian, MDGregory T. Simonian, MD – FDA Inspection, Dec 11, 2012
Record Details
This FDA Inspection record concerns Gregory T. Simonian, MD, with an inspection on December 11, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Gregory T. Simonian, MD
- Inspection Date
- December 11, 2012
- Product Type
- Devices
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ID · 46cc48b2-304b-4536-811a-cb855ea72fd8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 811727
- 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)(2)(i)Investigator device accountability inadequate
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Other FDA inspections of Gregory T. Simonian, MD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 16, 2013 | NAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
| March 24, 2010 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Gregory T. Simonian, MD
- FDA Inspection 847749 - 2013-08-16
- FDA Inspection 653614 - 2010-03-24
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