FDA Inspection 1062912 - Joimax GmbH - July 04, 2018

Record Details

This FDA Inspection record concerns Joimax GmbH, with an inspection on July 4, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Joimax GmbH
Inspection Date: July 4, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c851c902-b39f-4eea-963d-4904acbf62d6