# Guidewire Technologies, Inc., Salem, NH – FDA Inspections

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. 7 FDA inspections on record (1 OAI), last inspected March 28, 2025.

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## Details

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

## Related Documents

- FDA Inspection 1267030 - Guidewire Technologies, Inc. - 2025-03-28 — source: FDA, date: March 28, 2025
- FDA Inspection 1267030 - Guidewire Technologies, Inc. - 2025-03-28 — 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 — 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 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 5, 2008
- FDA Inspection 557517 - Guidewire Technologies, Inc. - 2008-11-05 — classification: No Action Indicated (NAI), source: FDA, date: November 5, 2008

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