FDA Inspection 946357 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 3011714312

The FDA completed an inspection of Oklahoma Blood Institute on Oct 6, 2015 in Little Rock, AR. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 6, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Little Rock, AR (United States)