FDA Inspection
UnityPoint Health Des Moines IRBUnityPoint Health Des Moines IRB – FDA Inspection, May 19, 2011
Record Details
This FDA Inspection record concerns UnityPoint Health Des Moines IRB, with an inspection on May 19, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- May 19, 2011
- Product Type
- Devices
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ID · 4961a653-6cc2-40b6-9161-95c16476acff
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 725218
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 56.108(a)(1)Initial and continuing reviews
Full citation text and observation details available on the Dashboard.
Other FDA inspections of UnityPoint Health Des Moines IRB
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 24, 2022 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| August 11, 2017 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for UnityPoint Health Des Moines IRB
- FDA Inspection 1178378 - 2022-08-24
- FDA Inspection 1021242 - 2017-08-11
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