FDA Inspection 1201673 — National Marrow Donor Program IRB

National Marrow Donor Program IRB — FEI 3005043090

The FDA completed an inspection of National Marrow Donor Program IRB on April 4, 2023 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 4, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

IRB

Citations

IDCFRDescription
730521 CFR 56.110(b)(2)Minor changes