FDA Inspection 1110454 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3012310498

The FDA completed an inspection of Octapharma Plasma, Inc. on November 4, 2019 in Grand Prairie, TX. 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 4, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grand Prairie, TX (United States)