FDA Inspection 1314856 — CSL Plasma Inc

CSL Plasma Inc — FEI 3023209390

The FDA completed an inspection of CSL Plasma Inc on Apr 29, 2026 in Milwaukee, WI. 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
Apr 29, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Milwaukee, WI (United States)

Citations

IDCFRDescription
923821 CFR 630.40(b)(3)Results of testing

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