FDA Inspection 1151448 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007899522

The FDA completed an inspection of Octapharma Plasma, Inc. on August 12, 2021 in Richmond, VA. 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 12, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Richmond, VA (United States)