FDA issued a Warning Letter to Guidewire Technologies, Inc. on 2/26/2010 as a result of this inspection.
483 Guidewire Technologies Jan 2010

483 Guidewire Technologies Jan 2010

Paul Geraci FDA, Abby Pelletier FDA$119.00 - Available Now

FDA investigators audited the Guidewire Technologies - Salem, NH, United States facility and issued inspectional observations (via FDA 483) on 22 Jan 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 22 Jan 2010
  • Location: Salem, United States
  • FEI: 1221806
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