FDA Inspection 1040193 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 3003949970

The FDA completed an inspection of Oklahoma Blood Institute on Dec 7, 2017 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
Dec 7, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Tulsa, OK (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.