# FDA Inspection 1062912 - Joimax GmbH - July 04, 2018

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

> FDA Inspection 1062912 for Joimax GmbH on July 04, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1062912 - 2018-07-04](https://www.globalkeysolutions.net/records/fda_inspections/joimax-gmbh/969eaa9a-1914-4820-966c-678d27867567)

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

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