FDA Inspection 1097594 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 3011893716

The FDA completed an inspection of CSL Plasma Inc. on July 18, 2019 in Columbus, OH. 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 18, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Columbus, OH (United States)

Citations

IDCFRDescription
1808121 CFR 630.10(e)(1)Medical Assessment Factors