# FDA Inspection 730676 - Lumitex Medical Devices Inc - June 22, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/fd30936b-0871-428a-aaea-5cebe0e06c04/
Source feed: FDA_Inspections

> FDA Inspection 730676 for Lumitex Medical Devices Inc on June 22, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 730676
- Company Name: Lumitex Medical Devices Inc
- Inspection Date: 2011-06-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/lumitex-medical-devices-inc/19fa724c-17a2-4f62-a576-8e27c8b303d1

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