# CURALLUX LLC – FDA Inspection, Aug 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/curallux-llc/4f84f5dc-8389-4afc-a6e5-3353adaeab49
Source feed: FDA_Inspections

> FDA inspection 1031449 of CURALLUX LLC, August 09, 2017. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031449
- Company Name: CURALLUX LLC
- Inspection Date: 2017-08-09
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Florida District Office
- Citation Count: 0

## Related Documents

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- [FDA Inspection 1086640 - 2019-04-17](https://www.keypedia.com/records/fda_inspections/curallux-llc/c17b0396-9edb-4fa6-977c-0d9468ebc04a)
- [FDA Inspection 971370 - 2016-05-10](https://www.keypedia.com/records/fda_inspections/curallux-llc/a75fce9d-ada1-4109-827f-28cd54ea2588)
- [FDA Inspection 900767 - 2014-11-07](https://www.keypedia.com/records/fda_inspections/curallux-llc/9055b9f3-cce2-4412-b150-a9458f2bbe97)
- [FDA Inspection 829251 - 2013-05-16](https://www.keypedia.com/records/fda_inspections/curallux-llc/db966d03-b1aa-4de7-aa1d-c0f1435055cd)

Company: https://www.keypedia.com/companies/curallux-llc/3b34bff1-b04e-407d-b872-763d34e20103

Office: https://www.keypedia.com/offices/florida-district-office/95b2a118-0b78-46e0-a54c-982bd7ce51c9