FDA Inspection 981325 - ACP - July 08, 2016

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Record Details

This FDA Inspection record concerns ACP, with an inspection on July 8, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: ACP
Inspection Date: July 8, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a265369b-c70c-4e06-ba46-932ed85e59cb

Violation Codes3

21 CFR 820.18421 CFR 820.70(i)21 CFR 820.75(a)

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