FDA Inspection 824137 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3008166892

The FDA completed an inspection of Octapharma Plasma, Inc. on Mar 21, 2013 in Fort Worth, TX. 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
Mar 21, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Worth, TX (United States)