FDA Inspection 1031336 - Westone Laboratories, Inc. - November 15, 2017

Record Details

This FDA Inspection record concerns Westone Laboratories, Inc., with an inspection on November 15, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Westone Laboratories, Inc.
Inspection Date: November 15, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1d633c1c-c2c4-4012-8943-3fc03566752c

Violation Codes3

21 CFR 820.198(a)21 CFR 820.20(b)21 CFR 820.70(g)(1)

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