FDA Inspection 800085 - Gynex Corporation - September 21, 2012

FDA Inspection 800085 for Gynex Corporation on September 21, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 800085 for Gynex Corporation on September 21, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

Gynex Corporation

Inspection Date

September 21, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe90ccad-a7fd-47a2-b5c0-4c088d755c06

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