FDA Inspection
Ara Dikranian, MDAra Dikranian, MD – FDA Inspection, Aug 4, 2011
Record Details
This FDA Inspection record concerns Ara Dikranian, MD, with an inspection on August 4, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Ara Dikranian, MD
- Inspection Date
- August 4, 2011
- Product Type
- Drugs
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ID · 783f6612-ee48-459e-9a92-6c3eee180723
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 738336
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 312.66Unanticipated problems
- 21 CFR 50.25(a)(5)Confidentiality, FDA inspection of records
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Other FDA inspections of Ara Dikranian, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2008 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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