# Guidewire Technologies, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/guidewire-technologies-inc/7bc5f458-8c4c-4b85-8a6a-9ea29842d8aa

> Inspection records and compliance data for Guidewire Technologies, Inc. in Salem, New Hampshire. Access full analysis and detailed observations.

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## Details

- Name: Guidewire Technologies, Inc.
- FEI Number: 1221806
- City: Salem
- State: New Hampshire
- Country Name: United States
- Address Line 1: 26 Keewaydin Dr
- Zip Code: 03079

## Related Documents

- [FDA Inspection 1267030 - Guidewire Technologies, Inc. - 2025-03-28](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/cdefe96a-aa0b-4a4c-bda7-636ffefdb6c0) — source: FDA, date: March 28, 2025
- [FDA Inspection 1267030 - Guidewire Technologies, Inc. - 2025-03-28](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/362e49f4-fdac-4a4a-b7f6-25ccd278b8f8) — classification: No Action Indicated (NAI), source: FDA, date: March 28, 2025
- [FDA Inspection 963384 - Guidewire Technologies, Inc. - 2016-03-10](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/2db0e975-66ca-4ba1-8f73-f85de8a961d7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2016
- [FDA Inspection 903156 - Guidewire Technologies, Inc. - 2014-11-19](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/416633f2-65ca-4d76-aca4-2e5cabef77a2) — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2014
- [FDA Inspection 794870 - Guidewire Technologies, Inc. - 2012-08-16](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/b6e66120-1415-42d3-8f47-f68a4c1096bb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 16, 2012
- [FDA Inspection 678089 - Guidewire Technologies, Inc. - 2010-08-12](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/9434e848-ce91-42a9-942c-9130b9515983) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 12, 2010
- [FDA Inspection 644227 - Guidewire Technologies, Inc. - 2010-01-22](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/9bfc53dc-1d6c-4566-afcb-d054e7ffe97b) — classification: Official Action Indicated (OAI), source: FDA, date: January 22, 2010
- [FDA Inspection 557517 - Guidewire Technologies, Inc. - 2008-11-05](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/38e7dc87-5bd8-4a07-a4bd-d9ff9d4fcc4f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 5, 2008
- [FDA Inspection 557517 - Guidewire Technologies, Inc. - 2008-11-05](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/958e6795-b579-4467-bcd0-620bbc673272) — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2008

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