FDA Inspection 1020733 - Heinz Kurz GmbH Medizintechnik - August 03, 2017

Record Details

This FDA Inspection record concerns Heinz Kurz GmbH Medizintechnik, with an inspection on August 3, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Heinz Kurz GmbH Medizintechnik
Inspection Date: August 3, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · db6e6f0d-3f45-435b-b97d-fd2d0d9a786c

Violation Codes1

21 CFR 820.70(i)

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