FDA issued a Warning Letter to Sanofi Pasteur on 6/30/2006 for a previous inspection.
483 Sanofi Pasteur May 2008

483 Sanofi Pasteur May 2008

Jacqueline Diaz Albert FDA, Mihaly Ligmond FDA$119.00 - Available Now

FDA investigators audited the Sanofi Pasteur - Swiftwater, PA, United States facility and issued inspectional observations (via FDA 483) on 16 May 2008.

Product details

  • Category: Biologics
  • Inspection end: 16 May 2008
  • Location: Swiftwater, United States
  • FEI: 2518760
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