FDA Inspection 1029562 — Mary Greeley Medical Center IRB

Mary Greeley Medical Center IRB — FEI 1931256

The FDA completed an inspection of Mary Greeley Medical Center IRB on July 12, 2017 in Ames, IA. 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
July 12, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ames, IA (United States)

Additional Details

IRB