FDA Inspection 977966 - Unitron Hearing Inc - January 12, 2016

FDA Inspection 977966 for Unitron Hearing Inc on January 12, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 977966 for Unitron Hearing Inc on January 12, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.100(b)

21 CFR 820.198(a)

21 CFR 820.20(c)

21 CFR 820.22

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Record Information

Company

Unitron Hearing Inc

Inspection Date

January 12, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff0d9001-3b96-41f2-8880-1146290ec894

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