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Beckman Coulter, Inc. 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 1017835.

Beckman Coulter, Inc.

Hialeah, Florida, United States
Issue DateJanuary 27, 2016
FEI Number1017835
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Beckman Coulter, Inc. FDA Form 483, Hialeah, Florida, January 27, 2016