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Vionic Group LLC 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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Vionic Group LLC

San Rafael, California, United States
Issue DateOctober 12, 2016
FEI Number3006795955
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Vionic Group LLC FDA Form 483, San Rafael, California, October 12, 2016