FDA Inspection 936910 - Verathon, Inc. - August 03, 2015

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Record Details

This FDA Inspection record concerns Verathon, Inc., with an inspection on August 3, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Verathon, Inc.
Inspection Date: August 3, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 625ca8d9-f8d2-4474-a735-086122be49bf

Violation Codes5

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(c)21 CFR 820.30(i)21 CFR 820.75(a)

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