FDA Inspection 727157 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 3003949970

The FDA completed an inspection of Oklahoma Blood Institute on May 27, 2011 in Tulsa, OK. 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
May 27, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tulsa, OK (United States)

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