VIVEVE DENVER Form 483 Details
Form 483Source: 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 3013565579.
VIVEVE DENVER
Englewood, Colorado, United States
Issue DateAugust 01, 2014
FEI Number3013565579
CountryUnited States
Status
No Warning LetterProduct Type
Devices