# FDA Inspection 903156 - Guidewire Technologies, Inc. - November 19, 2014

Source: https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/416633f2-65ca-4d76-aca4-2e5cabef77a2
Source feed: FDA_Inspections

> FDA Inspection 903156 for Guidewire Technologies, Inc. on November 19, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 903156
- Company Name: Guidewire Technologies, Inc.
- Inspection Date: 2014-11-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7