FDA Inspection 586007 - EDM International - June 03, 2009

FDA Inspection 586007 for EDM International on June 03, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 586007 for EDM International on June 03, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

EDM International

Inspection Date

June 3, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9b83cda-3ad9-45b5-a673-815cde081455

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