# FDA Inspection 960542 - University of Michigan Health West IRB - January 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/university-of-michigan-health-west-irb/28731389-5582-485d-98e2-c40faf5e4e9b
Source feed: FDA_Inspections

> FDA Inspection 960542 for University of Michigan Health West IRB on January 21, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960542
- Company Name: University of Michigan Health West IRB
- Inspection Date: 2016-01-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1167527 - 2022-04-07](https://www.keypedia.com/records/fda_inspections/university-of-michigan-health-west-irb/28f4f5b2-c413-43b9-8fd8-f5d02a1cca27)

Company: https://www.keypedia.com/companies/university-of-michigan-health-west-irb/df00deaf-3e14-4735-94b4-8aed3114d0b3

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7