FDA Inspection 1116508 — Octapharma Plasma, Inc. - Norfolk

Octapharma Plasma, Inc. - Norfolk — FEI 3007113703

The FDA completed an inspection of Octapharma Plasma, Inc. - Norfolk on Dec 5, 2019 in Norfolk, VA. 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
Dec 5, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Norfolk, VA (United States)

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