# neuroConn GmbH – FDA Inspection, Nov 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/neuroconn-gmbh/aead4a75-96af-431b-88f5-2336d7b20642
Source feed: FDA_Inspections

> FDA inspection 1031057 of neuroConn GmbH, November 09, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031057
- Company Name: neuroConn GmbH
- Inspection Date: 2017-11-09
- 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: 2

## Related Documents

- FDA Inspection 1298214 - 2025-12-09
- [FDA Inspection 1195429 - 2023-01-12](https://www.keypedia.com/records/fda_inspections/neuroconn-gmbh/c3e8c884-dcbb-4a1a-85e9-dfd9b6a1b476)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/neuroconn-gmbh/4b1f0293-1279-4534-9178-ced92e6fbbd8

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