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FDA Inspection 606585 — Oklahoma Blood Institute Northwest

Oklahoma Blood Institute Northwest — FEI 1626218

The FDA completed an inspection of Oklahoma Blood Institute Northwest on August 13, 2009 in Enid, 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
August 13, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Enid, OK (United States)

Facility

Other inspections at this facility

  • 1199216 (NAI Fri Feb 24 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1068531 (NAI Wed Sep 19 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 976726 (NAI Thu May 12 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 856152 (NAI Wed Nov 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 756042 (NAI Fri Dec 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources