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Cerner Enviza LLC 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 1931259.

Cerner Enviza LLC

Kansas City, Missouri, United States
Issue DateJune 01, 2010
FEI Number1931259
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Cerner Enviza LLC FDA Form 483, Kansas City, Missouri, June 1, 2010