FDA Inspection 805215 — CSL Plasma, Inc.

CSL Plasma, Inc. — FEI 1000517678

The FDA completed an inspection of CSL Plasma, Inc. on October 19, 2012 in Fort Collins, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 19, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Collins, CO (United States)

Citations

IDCFRDescription
25521 CFR 640.31Donor eligibility
9821 CFR 606.100(c)Thorough investigations