FDA Inspection 1284988 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 3003949970

The FDA completed an inspection of Oklahoma Blood Institute on Aug 26, 2026 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
Aug 26, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tulsa, OK (United States)

Citations

IDCFRDescription
442521 CFR 606.60(a)Equipment observed, standardized, calibrated

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