# Guidewire Technologies, Inc. – FDA Inspection, Mar 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/guidewire-technologies-inc/2db0e975-66ca-4ba1-8f73-f85de8a961d7
Source feed: FDA_Inspections

> FDA inspection 963384 of Guidewire Technologies, Inc., March 10, 2016. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 963384
- Company Name: Guidewire Technologies, Inc.
- Inspection Date: 2016-03-10
- 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: 3

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- [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)
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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