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Simex Medizintechnik 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 3005813597.

Simex Medizintechnik Gmbh

Deislingen, -, Germany
Issue DateNovember 15, 2017
FEI Number3005813597
CountryGermany
Status
No Warning Letter
Product Type
Devices
Simex Medizintechnik Gmbh FDA Form 483, Deislingen, November 15, 2017