FDA Inspection
Virtua IRBVirtua IRB – FDA Inspection, Feb 25, 2009
Record Details
This FDA Inspection record concerns Virtua IRB, with an inspection on February 25, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Virtua IRB
- Inspection Date
- February 25, 2009
- Product Type
- Devices
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ID · 6c7c6ed6-d2e2-4cf6-8050-dd3da60a8402
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 566490
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 56.115(a)(4)Copies of IRB/CI correspondence
- 21 CFR 56.115(a)(6)Written procedures per 56.108(a) and (b)
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Other FDA inspections of Virtua IRB
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 6, 2025 | Not classified | New Jersey District Office | |
| September 25, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| November 14, 2013 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Virtua IRB
- FDA Inspection 1272587 - 2025-06-06
- FDA Inspection 1081934 - 2018-09-25
- FDA Inspection 854352 - 2013-11-14
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