# FDA Inspection 639866 - Isolux, LLC - January 22, 2010

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

> FDA Inspection 639866 for Isolux, LLC on January 22, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 639866
- Company Name: Isolux, LLC
- Inspection Date: 2010-01-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 984872 - 2016-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/isolux-llc/4bc6a64a-49ad-40ba-885e-4910e33629b6/)
- [FDA Inspection 984872 - 2016-09-14](https://www.globalkeysolutions.net/api/records/fda_inspections/isolux-llc/44021cf7-17b5-4114-965a-e2fab0f2e893/)
- [FDA Inspection 948806 - 2015-11-06](https://www.globalkeysolutions.net/api/records/fda_inspections/isolux-llc/a4f7b098-fea9-4b8f-b64d-72aa54075212/)
- [FDA Inspection 948806 - 2015-11-06](https://www.globalkeysolutions.net/api/records/fda_inspections/isolux-llc/448145a0-92ce-4561-8625-2861c5478fc8/)
- [FDA Inspection 639866 - 2010-01-22](https://www.globalkeysolutions.net/api/records/fda_inspections/isolux-llc/2033e975-d8e5-464d-bb24-508a0f9a33e2/)

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

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