FDA Inspection 1095739 - The Lebanon Corporation, Inc. - June 28, 2019

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Record Details

This FDA Inspection record concerns The Lebanon Corporation, Inc., with an inspection on June 28, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Lebanon Corporation, Inc.
Inspection Date: June 28, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · eca3785e-c295-49bd-96a1-83a4a091c785

Violation Codes2

21 CFR 820.198(a)21 CFR 820.30(g)

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