FDA Inspection 604816 — GlaxoSmithKline Vaccines Srl

GlaxoSmithKline Vaccines Srl — FEI 3006738517

The FDA completed an inspection of GlaxoSmithKline Vaccines Srl on Jul 31, 2009 in Sovicille. 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
Jul 31, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Sovicille (Italy)

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