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FDA Inspection 712920 — Baxalta Belgium Manufacturing SA

Baxalta Belgium Manufacturing SA — FEI 3002806503

The FDA completed an inspection of Baxalta Belgium Manufacturing SA on January 21, 2011 in Lessines. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Biologics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 21, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Lessines (Belgium)

Facility

Other inspections at this facility

  • 1251969 (VAI Fri Nov 22 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1093550 (VAI Fri May 31 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 918229 (VAI Tue Feb 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841219 (NAI Tue Jun 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 827427 (VAI Tue Mar 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources