FDA Inspection 1193146 - Louisville APL Diagnostics, Inc. - December 19, 2022

FDA Inspection 1193146 for Louisville APL Diagnostics, Inc. on December 19, 2022. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1193146 for Louisville APL Diagnostics, Inc. on December 19, 2022. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Louisville APL Diagnostics, Inc.

Inspection Date

December 19, 2022

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f91083fb-a846-40ab-84fd-3059a8a215d1

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