FDA Inspection 1130508 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3012201271

The FDA completed an inspection of Octapharma Plasma, Inc. on September 11, 2020 in Baltimore, MD. 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
September 11, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Baltimore, MD (United States)