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 Jun 18, 2010 in Siena. 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). Product area: Biologics.

Inspection details

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

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