FDA Inspection 996283 - Meko - January 06, 2017

Record Details

This FDA Inspection record concerns Meko, with an inspection on January 6, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Meko
Inspection Date: January 6, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 2d2b0164-faf9-4213-a877-968af2437306