FDA Inspection 1259244 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006295572

The FDA completed an inspection of Octapharma Plasma, Inc. on Dec 13, 2024 in Lynchburg, VA. 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
Dec 13, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lynchburg, VA (United States)

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