FDA Inspection 1144543 — Advarra IRB

Advarra IRB — FEI 3002908905

The FDA completed an inspection of Advarra IRB on May 27, 2021 in Columbia, MD. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 27, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Columbia, MD (United States)

Additional Details

IRB