FDA Inspection 887635 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007855568

The FDA completed an inspection of Octapharma Plasma, Inc. on Jun 30, 2014 in Kalamazoo, MI. 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
Jun 30, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Kalamazoo, MI (United States)

Citations

IDCFRDescription
9821 CFR 606.100(c)Thorough investigations