FDA Inspection 1024231 - Defibtech, LLC - August 16, 2017

Record Details

This FDA Inspection record concerns Defibtech, LLC, with an inspection on August 16, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Defibtech, LLC
Inspection Date: August 16, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 56a79898-db85-41bd-a509-14bf67ac81b9