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Ivoclar Vivadent AG Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3002808636.

Ivoclar Vivadent AG

Schaan, -, Liechtenstein
Issue DateAugust 24, 2016
FEI Number3002808636
CountryLiechtenstein
Status
No Warning Letter
Product Type
Devices
Ivoclar Vivadent AG FDA Form 483, Schaan, August 24, 2016