# Futrex Tech, Inc. – FDA Inspection, Jan 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/futrex-tech-inc/489a93e8-2230-4643-9895-f81f71c2cb17
Source feed: FDA_Inspections

> FDA inspection 559035 of Futrex Tech, Inc., January 23, 2009. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 559035
- Company Name: Futrex Tech, Inc.
- Inspection Date: 2009-01-23
- 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: 4

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- [FDA Inspection 804015 - 2012-11-05](https://www.keypedia.com/records/fda_inspections/futrex-tech-inc/f3ad263e-6c33-4b85-b1ad-e0881bfa5e29)

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