# FDA Inspection 962772 - Vincent Systems Gmbh - January 21, 2016

Source: https://www.keypedia.com/records/fda_inspections/vincent-systems-gmbh/cfe509dc-9673-4147-a351-24038a2a01db
Source feed: FDA_Inspections

> FDA Inspection 962772 for Vincent Systems Gmbh on January 21, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 962772
- Company Name: Vincent Systems Gmbh
- Inspection Date: 2016-01-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 962772 - 2016-01-21](https://www.keypedia.com/records/fda_inspections/vincent-systems-gmbh/367d97fc-fa42-4d20-92b6-d3342607fe42)

Company: https://www.keypedia.com/companies/vincent-systems-gmbh/2c5d42bf-0a28-45a5-9ba3-66f6134e0919

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