# CURALLUX LLC – FDA Inspection, May 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/curallux-llc/a75fce9d-ada1-4109-827f-28cd54ea2588
Source feed: FDA_Inspections

> FDA inspection 971370 of CURALLUX LLC, May 10, 2016. Classification: Voluntary Action Indicated (VAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971370
- Company Name: CURALLUX LLC
- Inspection Date: 2016-05-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7