# DMX IMAGING, LLC – FDA Inspection, Jun 20, 2013

Source: https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/7c666f6f-d47a-451f-a87c-44d5719d2f3c
Source feed: FDA_Inspections

> FDA inspection 836771 of DMX IMAGING, LLC, June 20, 2013. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 836771
- Company Name: DMX IMAGING, LLC
- Inspection Date: 2013-06-20
- 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 Documents

- [FDA Inspection 1033872 - 2017-12-04](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/6dafadc8-6d06-4bb0-89e0-91a100b20e5c)
- FDA Inspection 929787 - 2015-06-05
- [FDA Inspection 785658 - 2012-06-07](https://www.keypedia.com/records/fda_inspections/dmx-imaging-llc/ffe2ff98-51f9-4e5c-b5d7-5580f5bd63df)

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