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Maquet Cardiopulmonary 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 3004752057.

Maquet Cardiopulmonary Ag

Hirrlingen, -, Germany
Issue DateJanuary 10, 2014
FEI Number3004752057
CountryGermany
Status
No Warning Letter
Product Type
Devices
Maquet Cardiopulmonary Ag FDA Form 483, Hirrlingen, January 10, 2014