Company
United StatesUnityPoint Health Des Moines IRB, Des Moines, IA – FDA Inspections
Inspection records and compliance data for UnityPoint Health Des Moines IRB in Des Moines, Iowa. 3 FDA inspections on record, 1 Form 483, last inspected August 24, 2022.
Company Profile
This profile covers UnityPoint Health Des Moines IRB based in Des Moines, Iowa, United States.
FDA Inspection History
- FDA inspections
- 3
- OAI
- 0
- VAI
- 2
- NAI
- 1
- Form 483s
- 1
- Warning letters
- 0
First inspected May 19, 2011. Last inspected August 24, 2022.
Most cited issue areas
- Initial and continuing reviews1 inspection
- Prompt reporting of noncompliance1 inspection
FDA inspections (3)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| August 24, 2022 | NAI | Human Drugs · Bioresearch Monitoring | 1178378 |
| August 11, 2017 | VAI | Medical Devices & Rad Health · Bioresearch Monitoring | 1021242 |
| May 19, 2011 | VAI | Medical Devices & Rad Health · Bioresearch Monitoring | 725218 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
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Company Information
Name
UnityPoint Health Des Moines IRB
FEI Number
3000717839
Address
700 E University Ave, Des Moines, Iowa 50316, United States
Country
United States
ID: cd56f585-f65f-43a4-93c9-14ca7fc45699