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Sivantos GmbH 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 3005019184.

Sivantos GmbH

Erlangen, -, Germany
Issue DateOctober 31, 2013
FEI Number3005019184
CountryGermany
Status
No Warning Letter
Product Type
Devices
Sivantos GmbH FDA Form 483, Erlangen, October 31, 2013