FDA issued a Warning Letter to Genzyme Corporation on 2/27/2009 for a previous inspection.
483 Sanofi Genzyme Nov 2009

483 Sanofi Genzyme Nov 2009

Thomas Arista FDA, Debra Emerson FDA$119.00 - Available Now

FDA investigators audited the Sanofi Genzyme - Allston, MA, United States facility and issued inspectional observations (via FDA 483) on 13 Nov 2009.

Product details

  • Category: Human Drugs
  • Inspection end: 13 Nov 2009
  • Location: Allston, United States
  • FEI: 1000305672
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