Company
United StatesU Of MN Research Subjects' Protection Program/ IRB, Minneapolis, MN – FDA Inspections
Inspection records and compliance data for U Of MN Research Subjects' Protection Program/ IRB in Minneapolis, Minnesota. 4 FDA inspections on record, last inspected May 28, 2025.
Company Profile
This profile covers U Of MN Research Subjects' Protection Program/ IRB based in Minneapolis, Minnesota, United States.
FDA Inspection History
- FDA inspections
- 4
- OAI
- 0
- VAI
- 2
- NAI
- 2
- Form 483s
- 0
- Warning letters
- 0
First inspected October 18, 2011. Last inspected May 28, 2025.
Most cited issue areas
- Initial and continuing reviews2 inspections
FDA inspections (4)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| May 28, 2025 | NAI | Biologics, Human Drugs, Medical Devices & Rad Health · Bioresearch Monitoring | 1272387 |
| December 12, 2019 | NAI | Human Drugs, Medical Devices & Rad Health · Bioresearch Monitoring | 1115377 |
| September 25, 2015 | VAI | Human Drugs · Bioresearch Monitoring | 945720 |
| October 18, 2011 | VAI | Medical Devices & Rad Health · Bioresearch Monitoring | 749422 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
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TriHealth IRB
Lakeland Regional Health Systems Inc.
Ascension St. John Hospital IRB
Washington University Human Research Protections Office
Company Information
Name
U Of MN Research Subjects' Protection Program/ IRB
FEI Number
2127205
Address
Macnamara Alumni Center, 200 Oak St Se Ste 350-2, Minneapolis, Minnesota 55455, United States
Country
United States
ID: e204f5fb-1d82-47a7-925d-85736aaa844f