# FDA Inspection 1021242 - UnityPoint Health Des Moines IRB - August 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/unitypoint-health-des-moines-irb/e5d5e789-71ae-4714-9a47-8788c4d5108e
Source feed: FDA_Inspections

> FDA Inspection 1021242 for UnityPoint Health Des Moines IRB on August 11, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021242
- Company Name: UnityPoint Health Des Moines IRB
- Inspection Date: 2017-08-11
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/unitypoint-health-des-moines-irb/cd56f585-f65f-43a4-93c9-14ca7fc45699

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