FDA Inspection 824557 - GyNova, LLC - March 26, 2013

FDA Inspection 824557 for GyNova, LLC on March 26, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 824557 for GyNova, LLC on March 26, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

GyNova, LLC

Inspection Date

March 26, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f898f783-0e33-41db-a511-8ddd519090d4

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