FDA Inspection 984370 — GlaxoSmithKline Research & Development Limited

GlaxoSmithKline Research & Development Limited — FEI 3003284850

The FDA completed an inspection of GlaxoSmithKline Research & Development Limited on Jun 24, 2016 in Stevenage. 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
Jun 24, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Stevenage (United Kingdom)

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