FDA inspection

Baxalta Belgium Manufacturing SA: FDA inspection ending Oct 19, 2009

FDA inspection 622355 · Official Action Indicated (OAI) · Lessines

Key facts

Inspection ID 622355
Firm Baxalta Belgium Manufacturing SA
FEI number 3002806503
Address Boulevard Rene Branquart 80
City Lessines
Country Belgium
Fiscal year 2010
Inspection end date Oct 19, 2009
Classification Official Action Indicated (OAI)
Project area Blood and Blood Products
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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