FDA Inspection 741058 — Octapharma Plasma, Inc. - Norfolk

Octapharma Plasma, Inc. - Norfolk — FEI 3007113703

The FDA completed an inspection of Octapharma Plasma, Inc. - Norfolk on Aug 15, 2011 in Norfolk, VA. 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 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

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