FDA Inspection 1215835 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3013154109

The FDA completed an inspection of Octapharma Plasma, Inc. on August 15, 2023 in Lansing, IL. 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
August 15, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Lansing, IL (United States)