FDA Inspection 905889 - Acteon, Inc. - December 10, 2014

Record Details

This FDA Inspection record concerns Acteon, Inc., with an inspection on December 10, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Acteon, Inc.
Inspection Date: December 10, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 7fc0adc6-924b-4c45-ad96-e8574b5ca69b

Violation Codes3

21 CFR 820.5021 CFR 820.70(a)21 CFR 820.80(b)

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