FDA Inspection 832578 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 1876561

The FDA completed an inspection of CSL Plasma Inc. on May 22, 2013 in W Lafayette, IN. 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
May 22, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
W Lafayette, IN (United States)

Citations

IDCFRDescription
904421 CFR 600.10(b)Personnel capabilities