FDA Inspection 1114822 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3019655

The FDA completed an inspection of Octapharma Plasma, Inc. on November 5, 2019 in Murray, UT. 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
November 5, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Murray, UT (United States)