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MaxiFlex, LLC 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 3006812215

MaxiFlex, LLC

New Orleans, Louisiana, United States
Issue DateDecember 20, 2018
FEI Number3006812215
CountryUnited States
Status
No Warning Letter
Product Type
Devices
MaxiFlex, LLC FDA Form 483, New Orleans, Louisiana, December 20, 2018