FDA Inspection 988253 - Ivoclar Vivadent AG - August 24, 2016

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Record Details

This FDA Inspection record concerns Ivoclar Vivadent AG, with an inspection on August 24, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Ivoclar Vivadent AG
Inspection Date: August 24, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 82a35996-096c-44d6-9368-f7db474ac5bc

Violation Codes1

21 CFR 820.198(a)

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