FDA Inspection
Acteon, Inc.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.
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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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