# Ara Dikranian, MD – FDA Inspection, Oct 31, 2008

Source: https://www.keypedia.com/records/fda_inspections/ara-dikranian-md/529500a1-bcd5-4919-b6cc-c330778bc28f
Source feed: FDA_Inspections

> FDA inspection 546338 of Ara Dikranian, MD, October 31, 2008. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 546338
- Company Name: Ara Dikranian, MD
- Inspection Date: 2008-10-31
- 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 738336 - 2011-08-04](https://www.keypedia.com/records/fda_inspections/ara-dikranian-md/783f6612-ee48-459e-9a92-6c3eee180723)

Company: https://www.keypedia.com/companies/ara-dikranian-md/642a8e5d-301c-49d5-8d8e-60384fd6f26f

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