FDA Inspection 810435 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 1626009

The FDA completed an inspection of Oklahoma Blood Institute on October 11, 2012 in Oklahoma City, OK. 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
October 11, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Oklahoma City, OK (United States)