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Novosource 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 3009946696.

Novosource Inc

Dayton, Ohio, United States
Issue DateMarch 28, 2014
FEI Number3009946696
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Novosource Inc FDA Form 483, Dayton, Ohio, March 28, 2014