# Isolux, LLC – FDA Inspection, Sep 14, 2016

Source: https://www.keypedia.com/records/fda_inspections/isolux-llc/4bc6a64a-49ad-40ba-885e-4910e33629b6
Source feed: FDA_Inspections

> FDA inspection 984872 of Isolux, LLC, September 14, 2016. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 984872
- Company Name: Isolux, LLC
- Inspection Date: 2016-09-14
- 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: 7

## Related Documents

- [FDA Inspection 948806 - 2015-11-06](https://www.keypedia.com/records/fda_inspections/isolux-llc/a4f7b098-fea9-4b8f-b64d-72aa54075212)
- [FDA Inspection 639866 - 2010-01-22](https://www.keypedia.com/records/fda_inspections/isolux-llc/fda501d2-f18f-475f-a659-0e1496c16c80)

Company: https://www.keypedia.com/companies/isolux-llc/c651c7d4-26e1-4eef-8290-9a6256d61702

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