FDA Inspection 796054 — Csl Plasma

Csl Plasma — FEI 1525349

The FDA completed an inspection of Csl Plasma on Aug 30, 2012 in Columbus, 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 30, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Columbus, OH (United States)

Citations

IDCFRDescription
922521 CFR 606.171Biological product deviation report