FDA Inspection 1122598 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3013003537

The FDA completed an inspection of Octapharma Plasma Inc on Mar 12, 2020 in Windcrest, TX. 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
Mar 12, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Windcrest, TX (United States)

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