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Bioptron 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 3003775404.

Bioptron AG

Wollerau, -, Switzerland
Issue DateNovember 02, 2017
FEI Number3003775404
CountrySwitzerland
Status
No Warning Letter
Product Type
Devices
Bioptron AG FDA Form 483, Wollerau, November 2, 2017