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Belimed 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 3003927243.

Belimed AG

Sulgen, -, Switzerland
Issue DateAugust 10, 2012
FEI Number3003927243
CountrySwitzerland
Status
No Warning Letter
Product Type
Devices
Belimed AG FDA Form 483, Sulgen, August 10, 2012