FDA Inspection 886173 — GSK LLC (GlaxoSmithKline)

GSK LLC (GlaxoSmithKline) — FEI 3006810568

The FDA completed an inspection of GSK LLC (GlaxoSmithKline) on June 3, 2014 in Collegeville, PA. 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
June 3, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Collegeville, PA (United States)

Additional Details

Sponsor, Contract Research Organization