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

Source: https://www.globalkeysolutions.net/records/fda_inspections/heinz-kurz-gmbh-medizintechnik/db6e6f0d-3f45-435b-b97d-fd2d0d9a786c
Source feed: FDA_Inspections

> FDA Inspection 1020733 for Heinz Kurz GmbH Medizintechnik on August 03, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020733
- Company Name: Heinz Kurz GmbH Medizintechnik
- Inspection Date: 2017-08-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/heinz-kurz-gmbh-medizintechnik/026648fc-9267-46e7-9546-b4191d2c1163

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7