FDA Inspection 1147871 — Octapharma Plasma Inc.

Octapharma Plasma Inc. — FEI 3016430495

The FDA completed an inspection of Octapharma Plasma Inc. on July 16, 2021 in San Antonio, 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
July 16, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
San Antonio, TX (United States)