FDA Inspection 1243718 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3012725455

The FDA completed an inspection of CSL Plasma Inc. on July 12, 2024 in Saginaw, MI. 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
July 12, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Saginaw, MI (United States)

Citations

IDCFRDescription
3521 CFR 606.40Clean & orderly