FDA Inspection 1114117 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3013453691

The FDA completed an inspection of Octapharma Plasma, Inc. on Nov 15, 2019 in Orlando, FL. 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
Nov 15, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Orlando, FL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.