FDA Inspection 668592 - Gyrus Acmi, In. - June 24, 2010

FDA Inspection 668592 for Gyrus Acmi, In. on June 24, 2010. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 668592 for Gyrus Acmi, In. on June 24, 2010. Classification: No Action Indicated (NAI).

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Record Information

Company

Gyrus Acmi, In.

Inspection Date

June 24, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f78824e5-4a3f-47ae-abc7-2a4966fc9a1d

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