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Nihon Kohden America LLC 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 2080783

Nihon Kohden America LLC

Irvine, California, United States
Issue DateApril 30, 2019
FEI Number2080783
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Nihon Kohden America LLC FDA Form 483, Irvine, California, April 30, 2019