FDA Inspection 1001740 - Edward M. Geltman, MD - January 30, 2017

FDA Inspection 1001740 for Edward M. Geltman, MD on January 30, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1001740 for Edward M. Geltman, MD on January 30, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Edward M. Geltman, MD

Inspection Date

January 30, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f991fb42-916b-4c39-9a62-e89891ee1b1e

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