FDA Inspection 1007184 — GlaxoSmithKline Biologicals SA

GlaxoSmithKline Biologicals SA — FEI 3002875226

The FDA completed an inspection of GlaxoSmithKline Biologicals SA on January 27, 2017 in Rixensart. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 27, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Rixensart (Belgium)