FDA issued a Warning Letter to Guidewire Technologies, Inc. on 2/26/2010 as a result of this inspection.
FDA investigators audited the Guidewire Technologies - Salem, NH, United States facility and issued inspectional observations (via FDA 483) on 22 Jan 2010.
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- Category: Medical Devices & Rad Health
- Inspection end: 22 Jan 2010
- Location: Salem, United States
- FEI: 1221806