FDA Inspection 741058 — Octapharma Plasma, Inc. - Norfolk

Octapharma Plasma, Inc. - Norfolk — FEI 3007113703

The FDA completed an inspection of Octapharma Plasma, Inc. - Norfolk on August 15, 2011 in Norfolk, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 15, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Norfolk, VA (United States)

Citations

IDCFRDescription
15521 CFR 606.160(b)Required records