FDA Inspection 813940 - Eisertech LLC - December 19, 2012

FDA Inspection 813940 for Eisertech LLC on December 19, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 813940 for Eisertech LLC on December 19, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Eisertech LLC

Inspection Date

December 19, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa5b6021-bfc3-4530-a8fe-563dabea9ce9

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