FDA Inspection 1231637 — Oklahoma Blood Institute

Oklahoma Blood Institute — FEI 1626009

The FDA completed an inspection of Oklahoma Blood Institute on Aug 20, 2024 in Oklahoma City, 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
Aug 20, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Oklahoma City, OK (United States)

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