FDA Inspection 1333734 — Octapharma Plasma, Inc

Octapharma Plasma, Inc — FEI 3030225339

The FDA completed an inspection of Octapharma Plasma, Inc on Aug 17, 2026 in Canton, OH. 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 17, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Canton, OH (United States)

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