FDA Inspection 979666 - The Lebanon Corporation, Inc. - May 05, 2016

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Record Details

This FDA Inspection record concerns The Lebanon Corporation, Inc., with an inspection on May 5, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: The Lebanon Corporation, Inc.
Inspection Date: May 5, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 20b405fb-c260-43d4-a055-5d5d20e8d853

Violation Codes7

21 CFR 820.100(a)21 CFR 820.198(c)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.50(a)(1)21 CFR 820.70(a)21 CFR 820.90(a)

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