FDA Inspection 547210 — CSL Plasma Inc.

CSL Plasma Inc. — FEI 2171832

The FDA completed an inspection of CSL Plasma Inc. on Nov 13, 2008 in Canton, OH. 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). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 13, 2008
Fiscal Year
2009
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Canton, OH (United States)

Citations

IDCFRDescription
7621 CFR 606.100(b)Establish, maintain and follow manufacturing SOPs
922521 CFR 606.171Biological product deviation report

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