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Ameriflo2 Incorporated 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 3013744387.

Ameriflo2 Incorporated

Indianapolis, Indiana, United States
Issue DateApril 16, 2013
FEI Number3013744387
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Ameriflo2 Incorporated FDA Form 483, Indianapolis, Indiana, April 16, 2013