FDA Inspection 1047796 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006295572

The FDA completed an inspection of Octapharma Plasma, Inc. on Mar 1, 2018 in Lynchburg, 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
Mar 1, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lynchburg, VA (United States)

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