FDA Inspection 839340 - Vitalograph (Ireland), Ltd. - May 23, 2013

FDA Inspection 839340 for Vitalograph (Ireland), Ltd. on May 23, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 839340 for Vitalograph (Ireland), Ltd. on May 23, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Vitalograph (Ireland), Ltd.

Inspection Date

May 23, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb29e501-31e6-4f0f-bd68-aee958a3826f

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