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Gentell, Inc Form 483 Details

Form 483
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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 1000522686

Gentell, Inc

Bristol, Pennsylvania, United States
Issue DateDecember 12, 2019
FEI Number1000522686
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Gentell, Inc FDA Form 483, Bristol, Pennsylvania, December 12, 2019