FDA issued a Warning Letter to Guidewire Technologies, Inc. on 2/26/2010 for a previous inspection.
483 Guidewire Technologies Mar 2016

483 Guidewire Technologies Mar 2016

James Whitney FDA$119.00 - Available Now

FDA investigators audited the Guidewire Technologies - Salem, NH, United States facility and issued 3 inspectional observations (via FDA 483) on 10 Mar 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 3
  • Inspection end: 10 Mar 2016
  • Location: Salem, United States
  • FEI: 1221806
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