FDA Inspection 1022919 - Neomend Inc - August 10, 2017

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Record Details

This FDA Inspection record concerns Neomend Inc, with an inspection on August 10, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Neomend Inc
Inspection Date: August 10, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 011214b3-bd4d-4440-b993-ead2fe55f92a