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Ventracor, 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.

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Ventracor, Inc

Budd Lake, New Jersey, United States
Issue DateApril 30, 2009
FEI Number3007471419
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Ventracor, Inc FDA Form 483, Budd Lake, New Jersey, April 30, 2009