# UnityPoint Health Des Moines IRB – FDA Inspection, Aug 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 of UnityPoint Health Des Moines IRB, August 11, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 56. Form 483 issued. 2 other FDA inspections on record for this company.

---

## 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)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1178378 - 2022-08-24
- [FDA Inspection 725218 - 2011-05-19](https://www.keypedia.com/records/fda_inspections/unitypoint-health-des-moines-irb/4961a653-6cc2-40b6-9161-95c16476acff)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/vickie-j-kanion/4ec38844-d90f-490e-bdfb-7bcee20fcc90)

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