# Isolux, LLC – FDA Inspection, Jan 22, 2010

Source: https://www.keypedia.com/records/fda_inspections/isolux-llc/fda501d2-f18f-475f-a659-0e1496c16c80
Source feed: FDA_Inspections

> FDA inspection 639866 of Isolux, LLC, January 22, 2010. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 639866
- Company Name: Isolux, LLC
- Inspection Date: 2010-01-22
- 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 984872 - 2016-09-14](https://www.keypedia.com/records/fda_inspections/isolux-llc/4bc6a64a-49ad-40ba-885e-4910e33629b6)
- [FDA Inspection 948806 - 2015-11-06](https://www.keypedia.com/records/fda_inspections/isolux-llc/a4f7b098-fea9-4b8f-b64d-72aa54075212)

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