FDA Inspection 907990 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007587556

The FDA completed an inspection of Octapharma Plasma, Inc. on December 15, 2014 in Lubbock, 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
December 15, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lubbock, TX (United States)