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Via Biomedical 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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Via Biomedical

Maple Grove, Minnesota, United States
Issue DateOctober 24, 2008
FEI Number3004152466
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Via Biomedical FDA Form 483, Maple Grove, Minnesota, October 24, 2008