# Guidewire Technologies, Inc. – FDA Inspection, Aug 12, 2010

Source: https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/9434e848-ce91-42a9-942c-9130b9515983
Source feed: FDA_Inspections

> FDA inspection 678089 of Guidewire Technologies, Inc., August 12, 2010. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 678089
- Company Name: Guidewire Technologies, Inc.
- Inspection Date: 2010-08-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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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