# Futrex Tech, Inc. – FDA Inspection, Nov 5, 2012

Source: https://www.keypedia.com/records/fda_inspections/futrex-tech-inc/f3ad263e-6c33-4b85-b1ad-e0881bfa5e29
Source feed: FDA_Inspections

> FDA inspection 804015 of Futrex Tech, Inc., November 05, 2012. Classification: Official Action Indicated (OAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 804015
- Company Name: Futrex Tech, Inc.
- Inspection Date: 2012-11-05
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 975765 - 2016-06-21
- FDA Inspection 836440 - 2013-06-17
- [FDA Inspection 559035 - 2009-01-23](https://www.keypedia.com/records/fda_inspections/futrex-tech-inc/489a93e8-2230-4643-9895-f81f71c2cb17)

Company: https://www.keypedia.com/companies/futrex-tech-inc/5603ac8b-208b-43e8-add4-a793c5117c77

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