FDA Inspection
Ara Dikranian, MDAra Dikranian, MD – FDA Inspection, Oct 31, 2008
Record Details
This FDA Inspection record concerns Ara Dikranian, MD, with an inspection on October 31, 2008, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Ara Dikranian, MD
- Inspection Date
- October 31, 2008
- Product Type
- Devices
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ID · 529500a1-bcd5-4919-b6cc-c330778bc28f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 546338
- 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)Investigator"s subject records inadequate
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Other FDA inspections of Ara Dikranian, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 4, 2011 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
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