FDA Inspection
CURALLUX LLCCURALLUX LLC – FDA Inspection, May 10, 2016
Record Details
This FDA Inspection record concerns CURALLUX LLC, with an inspection on May 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- CURALLUX LLC
- Inspection Date
- May 10, 2016
- Product Type
- Devices
View Company Profile
ID · a75fce9d-ada1-4109-827f-28cd54ea2588
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 971370
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of CURALLUX LLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 7, 2019 | Not classified | Florida District Office | |
| April 17, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 9, 2017 | Not classified | Florida District Office | |
| November 7, 2014 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 16, 2013 | OAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
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