FDA Inspection 1113152 — Octapharma Plasma Inc.

Octapharma Plasma Inc. — FEI 3011816220

The FDA completed an inspection of Octapharma Plasma Inc. on December 12, 2019 in Columbus, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 12, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Columbus, OH (United States)