FDA Inspection 800182 - FMS, Finapres Medical Systems BV - September 26, 2012

FDA Inspection 800182 for FMS, Finapres Medical Systems BV on September 26, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 800182 for FMS, Finapres Medical Systems BV on September 26, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

FMS, Finapres Medical Systems BV

Inspection Date

September 26, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffb53ed8-e4de-434b-a843-ac5a113a8645

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