FDA Inspection 1079836 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3013002390

The FDA completed an inspection of Octapharma Plasma, Inc. on Feb 6, 2019 in Fort Worth, TX. 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
Feb 6, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Worth, TX (United States)

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