FDA Inspection 1112107 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3005484053

The FDA completed an inspection of CSL Plasma Inc. on December 6, 2019 in Decatur, IL. 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
December 6, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Decatur, IL (United States)

Citations

IDCFRDescription
33321 CFR 640.64(e)Prevention of contamination