FDA Inspection 1331976 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 1071676

The FDA completed an inspection of Octapharma Plasma, Inc. on Aug 11, 2026 in Charlotte, 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
Aug 11, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Charlotte, NC (United States)

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