FDA Inspection
DMX IMAGING, LLCDMX IMAGING, LLC – FDA Inspection, Jun 20, 2013
Record Details
This FDA Inspection record concerns DMX IMAGING, LLC, with an inspection on June 20, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- DMX IMAGING, LLC
- Inspection Date
- June 20, 2013
- Product Type
- Devices
View Company Profile
ID · 7c666f6f-d47a-451f-a87c-44d5719d2f3c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 836771
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of DMX IMAGING, LLC
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 4, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 5, 2015 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| June 7, 2012 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for DMX IMAGING, LLC
- FDA Inspection 1033872 - 2017-12-04
- FDA Inspection 929787 - 2015-06-05
- FDA Inspection 785658 - 2012-06-07
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