# Domex Technology Corporation – FDA Inspection, Apr 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/domex-technology-corporation/9036322b-78d9-48bb-9199-7e84becedb22
Source feed: FDA_Inspections

> FDA inspection 1010435 of Domex Technology Corporation, April 12, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010435
- Company Name: Domex Technology Corporation
- Inspection Date: 2017-04-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/domex-technology-corporation/555c7e87-9507-4b84-8f8a-d2f1ced40438

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