# FDA Inspection 1010435 - Domex Technology Corporation - April 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/domex-technology-corporation/1d5c75c4-4f52-456f-a0c9-5fbe40468ca2
Source feed: FDA_Inspections

> FDA Inspection 1010435 for Domex Technology Corporation on April 12, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1010435 - 2017-04-12](https://www.keypedia.com/records/fda_inspections/domex-technology-corporation/9036322b-78d9-48bb-9199-7e84becedb22)

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