FDA Inspection 847629 — GlaxoSmithKline LLC

GlaxoSmithKline LLC — FEI 1000522100

The FDA completed an inspection of GlaxoSmithKline LLC on Aug 23, 2013 in King of Prussia, PA. 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: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 23, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
King of Prussia, PA (United States)

Additional details

Sponsor, Contract Research Organization

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