# Gregory T. Simonian, MD – FDA Inspection, Dec 11, 2012

Source: https://www.keypedia.com/records/fda_inspections/gregory-t-simonian-md/46cc48b2-304b-4536-811a-cb855ea72fd8
Source feed: FDA_Inspections

> FDA inspection 811727 of Gregory T. Simonian, MD, December 11, 2012. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 811727
- Company Name: Gregory T. Simonian, MD
- Inspection Date: 2012-12-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 847749 - 2013-08-16
- [FDA Inspection 653614 - 2010-03-24](https://www.keypedia.com/records/fda_inspections/gregory-t-simonian-md/c823161c-5e2e-4929-b569-e774a0310e92)

Company: https://www.keypedia.com/companies/gregory-t-simonian-md/36fc0565-e43b-46d7-bff5-bd85223ff049

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7