# FDA Inspection 598380 - Vygon US LLC d/b/a Vygon Neuro - June 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/vygon-us-llc-dba-vygon-neuro/e583a814-e84c-43e3-898c-fe80439c021d
Source feed: FDA_Inspections

> FDA Inspection 598380 for Vygon US LLC d/b/a Vygon Neuro on June 26, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 598380
- Company Name: Vygon US LLC d/b/a Vygon Neuro
- Inspection Date: 2009-06-26
- 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 598380 - 2009-06-26](https://www.keypedia.com/records/fda_inspections/vygon-us-llc-dba-vygon-neuro/c8f877b2-0c89-402b-8fdb-95fc9f1e9bb2)

Company: https://www.keypedia.com/companies/vygon-us-llc-dba-vygon-neuro/c1e0febe-44b2-4d19-b734-98a1ffc99cf3

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