# FDA Inspection 1172548 - Trinity Health Ann Arbor Hospital IRB - June 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/trinity-health-ann-arbor-hospital-irb/0b057741-3443-400a-acb8-6afa0d14225d
Source feed: FDA_Inspections

> FDA Inspection 1172548 for Trinity Health Ann Arbor Hospital IRB on June 08, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1172548
- Company Name: Trinity Health Ann Arbor Hospital IRB
- Inspection Date: 2022-06-08
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 888112 - 2014-07-21](https://www.keypedia.com/records/fda_inspections/trinity-health-ann-arbor-hospital-irb/a4ce59e1-5a77-442c-9a79-6139f363eb22)
- [FDA Inspection 715949 - 2011-03-18](https://www.keypedia.com/records/fda_inspections/trinity-health-ann-arbor-hospital-irb/02c6ae84-bc2d-4c38-8bb9-2bd5448825df)

Company: https://www.keypedia.com/companies/trinity-health-ann-arbor-hospital-irb/99489ac3-3d77-4810-9215-b85ae12caca3

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