FDA Inspection 1018343 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3008107480

The FDA completed an inspection of Octapharma Plasma, Inc. on March 1, 2017 in Garland, 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
March 1, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Garland, TX (United States)