FDA Inspection 1012564 - Louisville APL Diagnostics, Inc. - June 02, 2017

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Record Details

This FDA Inspection record concerns Louisville APL Diagnostics, Inc., with an inspection on June 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Louisville APL Diagnostics, Inc.
Inspection Date: June 2, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0e68a4ff-8148-4f3a-b062-841c23cf391e

Violation Codes2

21 CFR 820.198(e)21 CFR 820.70(b)

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