FDA Inspection 867537 - LumiQuick Diagnostics Inc. - February 24, 2014

FDA Inspection 867537 for LumiQuick Diagnostics Inc. on February 24, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 867537 for LumiQuick Diagnostics Inc. on February 24, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

LumiQuick Diagnostics Inc.

Inspection Date

February 24, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 2edc4fb4-f21f-4074-af46-e1202d4d215d

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