# FDA Inspection 1033872 - DMX IMAGING, LLC - December 04, 2017

Source: https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/226d3efc-ab98-4eaf-92d5-589e553579ad
Source feed: FDA_Inspections

> FDA Inspection 1033872 for DMX IMAGING, LLC on December 04, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1033872
- Company Name: DMX IMAGING, LLC
- Inspection Date: 2017-12-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1033872 - 2017-12-04](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/6dafadc8-6d06-4bb0-89e0-91a100b20e5c)
- [FDA Inspection 1033872 - 2017-12-04](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/090251d3-eb37-493a-91a4-a8b6598aee09)
- [FDA Inspection 929787 - 2015-06-05](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/978aeb48-321e-4b95-b850-3a8338f357f7)
- [FDA Inspection 929787 - 2015-06-05](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/5b9148fd-6387-41f0-ada3-567c02aff7a9)
- [FDA Inspection 929787 - 2015-06-05](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/9ba1121f-ab63-4e15-bd5a-a124afb03b00)

Company: https://www.keypedia.com/companies/dmx-imaging-llc/d4001d2a-7c43-43dd-b04a-687c4dd981f6

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