FDA Inspection 969894 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007587556

The FDA completed an inspection of Octapharma Plasma, Inc. on May 26, 2016 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
May 26, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lubbock, TX (United States)