FDA Inspection 683109 — GlaxoSmithKline Vaccines S.r.l.

GlaxoSmithKline Vaccines S.r.l. — FEI 3007780504

The FDA completed an inspection of GlaxoSmithKline Vaccines S.r.l. on June 18, 2010 in Siena. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 18, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Siena (Italy)