FDA Inspection 947463 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3008166892

The FDA completed an inspection of Octapharma Plasma, Inc. on Aug 10, 2015 in Fort Worth, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 10, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Worth, TX (United States)

Citations

IDCFRDescription
7521 CFR 606.100(a)SOP compliance