FDA Inspection 1017933 - Acuderm, Inc. - July 13, 2017

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Record Details

This FDA Inspection record concerns Acuderm, Inc., with an inspection on July 13, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Acuderm, Inc.
Inspection Date: July 13, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 97e26a06-4f30-4b31-bf40-4effa4018f92

Violation Codes5

21 CFR 820.100(b)21 CFR 820.198(a)21 CFR 820.2221 CFR 820.5021 CFR 820.72(a)

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