FDA Inspection 1191175 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3014127551

The FDA completed an inspection of Octapharma Plasma Inc on Nov 2, 2022 in Fife, WA. 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
Nov 2, 2022
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Fife, WA (United States)

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