FDA inspection

GlaxoSmithKline Biologicals SA: FDA inspection ending Jan 27, 2017

FDA inspection 1007184 · Voluntary Action Indicated (VAI) · Rixensart

Key facts

Inspection ID 1007184
Firm GlaxoSmithKline Biologicals SA
FEI number 3002875226
Address Rue de l'Institut 89
City Rixensart
Country Belgium
Fiscal year 2017
Inspection end date Jan 27, 2017
Classification Voluntary Action Indicated (VAI)
Project area Vaccines and Allergenic Products
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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