FDA Inspection 1158637 — GlaxoSmithKline Research & Development Limited

GlaxoSmithKline Research & Development Limited — FEI 3003284850

The FDA completed an inspection of GlaxoSmithKline Research & Development Limited on May 16, 2017 in Stevenage. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Stevenage (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)