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Virtex Form 483 Details

Form 483
View FDA's record for this firm
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 3009403270.

Virtex

Austin, Texas, United States
Issue DateSeptember 21, 2017
FEI Number3009403270
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Virtex FDA Form 483, Austin, Texas, September 21, 2017