FDA Inspection 861864 — Advarra IRB

Advarra IRB — FEI 3002908905

The FDA completed an inspection of Advarra IRB on January 7, 2014 in Columbia, MD. 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
January 7, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Columbia, MD (United States)

Additional Details

IRB