FDA Inspection 1113171 — Octapharma PLasma, Inc

Octapharma PLasma, Inc — FEI 3011935799

The FDA completed an inspection of Octapharma PLasma, Inc on November 21, 2019 in Milwaukee, WI. 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
November 21, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milwaukee, WI (United States)