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Genova Diagnostics 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 1000111208.

Genova Diagnostics

Asheville, North Carolina, United States
Issue DateFebruary 24, 2017
FEI Number1000111208
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Genova Diagnostics FDA Form 483, Asheville, North Carolina, February 24, 2017