# Heinz Kurz GmbH Medizintechnik – FDA Inspection, Aug 3, 2017

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

> FDA inspection 1020733 of Heinz Kurz GmbH Medizintechnik, August 03, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/thomas-e-friel/205f23ee-8648-46d1-8485-11977a27e8e4)

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

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