# FDA Inspection 1102799 - Neuromedex GmbH - September 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/neuromedex-gmbh/5cecfc9e-cfa0-438e-b05e-bca85fd2f2b4
Source feed: FDA_Inspections

> FDA Inspection 1102799 for Neuromedex GmbH on September 26, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102799
- Company Name: Neuromedex GmbH
- Inspection Date: 2019-09-26
- 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 1102799 - 2019-09-26](https://www.keypedia.com/records/fda_inspections/neuromedex-gmbh/aa79481e-ec8c-4f0c-93cf-626d74ce04ba)

Company: https://www.keypedia.com/companies/neuromedex-gmbh/66fe98ac-75e9-4f72-b3b9-c40a41744686

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