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Zenith Diagnostics Form 483 Details

Form 483
Find this 483 on FDA
Source: FDA Data DashboardFDA has published this inspection and the number of observations cited. The form itself has not been released yet, which usually takes six to twelve months.
Check this firm on FDA, establishment 3006493142

Zenith Diagnostics

Arlington Heights, Illinois, United States
Issue DateNovember 20, 2018
FEI Number3006493142
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Zenith Diagnostics FDA Form 483, Arlington Heights, Illinois, November 20, 2018