FDA Inspection 955238 — National Marrow Donor Program IRB

National Marrow Donor Program IRB — FEI 3005043090

The FDA completed an inspection of National Marrow Donor Program IRB on December 17, 2015 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 17, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Minneapolis, MN (United States)

Additional Details

IRB