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FDA Inspection 783865 — Sanofi Pasteur Limited

Sanofi Pasteur Limited — FEI 3002888623

The FDA completed an inspection of Sanofi Pasteur Limited on April 25, 2012 in North York. 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
April 25, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
North York (Canada)

Facility

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  • 1182359 (VAI Fri Oct 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1099275 (VAI Fri May 24 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 851779 (VAI Fri Sep 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources