# FDA Inspection 1267030 - Guidewire Technologies, Inc. - March 28, 2025

Source: https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/cdefe96a-aa0b-4a4c-bda7-636ffefdb6c0
Source feed: FDA_Inspections

> FDA Inspection 1267030 for Guidewire Technologies, Inc. on March 28, 2025. Classification: N/A.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267030
- Company Name: Guidewire Technologies, Inc.
- Inspection Date: 2025-03-28
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

## Related Documents

- [FDA Inspection 1267030 - 2025-03-28](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/362e49f4-fdac-4a4a-b7f6-25ccd278b8f8)
- [FDA Inspection 963384 - 2016-03-10](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/2db0e975-66ca-4ba1-8f73-f85de8a961d7)
- [FDA Inspection 903156 - 2014-11-19](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/416633f2-65ca-4d76-aca4-2e5cabef77a2)
- [FDA Inspection 794870 - 2012-08-16](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/b6e66120-1415-42d3-8f47-f68a4c1096bb)
- [FDA Inspection 678089 - 2010-08-12](https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/9434e848-ce91-42a9-942c-9130b9515983)

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

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144