FDA Inspection 1179353 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006718605

The FDA completed an inspection of Octapharma Plasma, Inc. on Sep 8, 2022 in Midfield, AL. 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
Sep 8, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Midfield, AL (United States)