FDA Inspection
Trident Health System IrbTrident Health System Irb – FDA Inspection, Jan 25, 2010
Record Details
This FDA Inspection record concerns Trident Health System Irb, with an inspection on January 25, 2010, covering devices.
- Company
- Trident Health System Irb
- Inspection Date
- January 25, 2010
- Product Type
- Devices
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ID · e0cf0f9c-9a4e-4815-94d2-00a8e6c696ce
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 640526
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
6- 21 CFR 56.115(a)(5)List of members
- 21 CFR 56.115(a)(1)Copies of all research proposals and related documents
- 21 CFR 56.115(a)(2)Minutes of IRB meetings
- 21 CFR 56.109(f)Continuing review
- 21 CFR 56.108(a)(1)Initial and continuing reviews
- 21 CFR 56.110(b)Research not eligible for expedited review
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Other FDA inspections of Trident Health System Irb
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Trident Health System Irb
- FDA Inspection 1058853 - 2018-06-21
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