FDA Inspection 1160764 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3015989031

The FDA completed an inspection of Octapharma Plasma Inc on Nov 5, 2021 in Raleigh, NC. 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 5, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Raleigh, NC (United States)

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