FDA Inspection 857250 - Dilon Medical Technologies Inc. - November 19, 2013

FDA Inspection 857250 for Dilon Medical Technologies Inc. on November 19, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 857250 for Dilon Medical Technologies Inc. on November 19, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Dilon Medical Technologies Inc.

Inspection Date

November 19, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff2cbbab-df4a-4172-91d7-f724e533e66e

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