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dBMEDx, Inc 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 3008321254.

dBMEDx, Inc

Littleton, Colorado, United States
Issue DateOctober 07, 2016
FEI Number3008321254
CountryUnited States
Status
No Warning Letter
Product Type
Devices
dBMEDx, Inc FDA Form 483, Littleton, Colorado, October 7, 2016