FDA Inspection 945317 - Menicon America, Inc. - August 26, 2015

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Record Details

This FDA Inspection record concerns Menicon America, Inc., with an inspection on August 26, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company: Menicon America, Inc.
Inspection Date: August 26, 2015
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 04db3900-2e62-486f-85dd-9b8cec9876be

Violation Codes3

21 CFR 820.100(a)(3)21 CFR 820.198(b)21 CFR 820.25(b)

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