# Joimax GmbH – FDA Inspection, Jul 4, 2018

Source: https://www.keypedia.com/records/fda_inspections/joimax-gmbh/c851c902-b39f-4eea-963d-4904acbf62d6
Source feed: FDA_Inspections

> FDA inspection 1062912 of Joimax GmbH, July 04, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062912
- Company Name: Joimax GmbH
- Inspection Date: 2018-07-04
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/joimax-gmbh/0cf6669f-acf8-4186-89b1-9d810b1dc822

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