FDA Inspection 1220574 - HertART ApS - August 28, 2023

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Record Details

This FDA Inspection record concerns HertART ApS, with an inspection on August 28, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: HertART ApS
Inspection Date: August 28, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8fcbc276-cb74-4b32-8e72-39f23675b2e0