FDA Inspection
University of Michigan Health West IRBUniversity of Michigan Health West IRB – FDA Inspection, Jan 21, 2016
Record Details
This FDA Inspection record concerns University of Michigan Health West IRB, with an inspection on January 21, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 21, 2016
- Product Type
- Devices
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ID · 28731389-5582-485d-98e2-c40faf5e4e9b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 960542
- 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 University of Michigan Health West IRB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 7, 2022 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for University of Michigan Health West IRB
- FDA Inspection 1167527 - 2022-04-07
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