FDA Inspection 1164256 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3019201803

The FDA completed an inspection of Octapharma Plasma, Inc. on Feb 16, 2022 in Wichita, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 16, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Wichita, KS (United States)