FDA Inspection 681145 - Ivoclar Vivadent Manufacturing GmbH - August 05, 2010

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Record Details

This FDA Inspection record concerns Ivoclar Vivadent Manufacturing GmbH, with an inspection on August 5, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Ivoclar Vivadent Manufacturing GmbH
Inspection Date: August 5, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0c25cc53-d485-4046-96c9-40342d88cd5b

Violation Codes2

21 CFR 820.250(b)21 CFR 820.70(b)

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