FDA Inspection 809900 - LumiQuick Diagnostics Inc. - December 07, 2012

Record Details

This FDA Inspection record concerns LumiQuick Diagnostics Inc., with an inspection on December 7, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: LumiQuick Diagnostics Inc.
Inspection Date: December 7, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · df045863-a951-4a3d-90b3-f5e3e2aae3b9

Violation Codes7

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.70(c)21 CFR 820.75(a)

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