FDA Inspection 1041438 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 1071676

The FDA completed an inspection of Octapharma Plasma, Inc. on January 11, 2018 in Charlotte, NC. 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
January 11, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Charlotte, NC (United States)