FDA Inspection
CURALLUX LLCCURALLUX LLC – FDA Inspection, Aug 9, 2017
Record Details
This FDA Inspection record concerns CURALLUX LLC, with an inspection on August 9, 2017, issued by the Florida District Office, covering medical devices & rad health.
- Company
- CURALLUX LLC
- Inspection Date
- August 9, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Florida District Office
View Company Profile
ID · 4f84f5dc-8389-4afc-a6e5-3353adaeab49
Inspection Facts
- Inspection number
- 1031449
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
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 |
| May 10, 2016 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
Other documents for CURALLUX LLC
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