FDA Inspection 945909 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 3003949970

The FDA completed an inspection of Oklahoma Blood Institute on Oct 16, 2015 in Tulsa, OK. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 16, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tulsa, OK (United States)

Citations

IDCFRDescription
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs

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