FDA Inspection
Trinity Health Ann Arbor Hospital IRBTrinity Health Ann Arbor Hospital IRB – FDA Inspection, Mar 18, 2011
Record Details
This FDA Inspection record concerns Trinity Health Ann Arbor Hospital IRB, with an inspection on March 18, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 18, 2011
- Product Type
- Devices
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ID · 02c6ae84-bc2d-4c38-8bb9-2bd5448825df
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 715949
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 56.115(a)(2)Minutes of IRB meetings
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Other FDA inspections of Trinity Health Ann Arbor Hospital IRB
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 8, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| July 21, 2014 | NAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
Other documents for Trinity Health Ann Arbor Hospital IRB
- FDA Inspection 1172548 - 2022-06-08
- FDA Inspection 888112 - 2014-07-21
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