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

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

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Record Summary

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

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Record Information

Company

Lumitex Medical Devices Inc

Inspection Date

June 22, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd30936b-0871-428a-aaea-5cebe0e06c04

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