# Isolux, LLC – FDA Inspection, Nov 6, 2015

Source: https://www.keypedia.com/records/fda_inspections/isolux-llc/a4f7b098-fea9-4b8f-b64d-72aa54075212
Source feed: FDA_Inspections

> FDA inspection 948806 of Isolux, LLC, November 06, 2015. Classification: Official Action Indicated (OAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 948806
- Company Name: Isolux, LLC
- Inspection Date: 2015-11-06
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 984872 - 2016-09-14](https://www.keypedia.com/records/fda_inspections/isolux-llc/4bc6a64a-49ad-40ba-885e-4910e33629b6)
- [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