# FDA Inspection 1093700 - MercyOne North Iowa Medical Center IRB - June 21, 2019

Source: https://www.keypedia.com/records/fda_inspections/mercyone-north-iowa-medical-center-irb/8c24f2df-6242-41e6-a081-0996238a189a
Source feed: FDA_Inspections

> FDA Inspection 1093700 for MercyOne North Iowa Medical Center IRB on June 21, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1093700
- Company Name: MercyOne North Iowa Medical Center IRB
- Inspection Date: 2019-06-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 863041 - 2014-01-16](https://www.keypedia.com/records/fda_inspections/mercyone-north-iowa-medical-center-irb/68f7af5e-d7a0-4c16-a5ae-7b2a21cb6613)
- [FDA Inspection 643582 - 2010-01-21](https://www.keypedia.com/records/fda_inspections/mercyone-north-iowa-medical-center-irb/d79228b1-5476-4e45-b57f-40d22ae53608)

Company: https://www.keypedia.com/companies/mercyone-north-iowa-medical-center-irb/11d8e28b-6d08-47e0-b865-08403f58e237

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