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Auxogyn 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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Auxogyn Inc.

Menlo Park, California, United States
Issue DateJune 01, 2016
FEI Number3009716149
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Auxogyn Inc. FDA Form 483, Menlo Park, California, June 1, 2016