# FDA Inspection 557517 - Guidewire Technologies, Inc. - November 05, 2008

Source: https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/38e7dc87-5bd8-4a07-a4bd-d9ff9d4fcc4f
Source feed: FDA_Inspections

> FDA Inspection 557517 for Guidewire Technologies, Inc. on November 05, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 557517
- Company Name: Guidewire Technologies, Inc.
- Inspection Date: 2008-11-05
- Classification: Voluntary Action Indicated (VAI)
- 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