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Beckman Coulter 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 3003766866.

Beckman Coulter GmbH

Marburg, -, Germany
Issue DateFebruary 02, 2017
FEI Number3003766866
CountryGermany
Status
No Warning Letter
Product Type
Devices
Beckman Coulter GmbH FDA Form 483, Marburg, February 2, 2017