# FDA Inspection 1258578 - Vygon Verneuil - December 19, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/vygon-verneuil/b1987f6c-434b-4e13-90a5-a90d6ebd293f
Source feed: FDA_Inspections

> FDA Inspection 1258578 for Vygon Verneuil on December 19, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258578
- Company Name: Vygon Verneuil
- Inspection Date: 2024-12-19
- 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 1258578 - 2024-12-19](https://www.globalkeysolutions.net/records/fda_inspections/vygon-verneuil/a291246d-fab3-45b2-ba79-239f1ed04945)
- [FDA Inspection 1258578 - 2024-12-19](https://www.globalkeysolutions.net/records/fda_inspections/vygon-verneuil/fd4573d5-3b1a-499b-aacb-0d4b3b12482b)

Company: https://www.globalkeysolutions.net/companies/vygon-verneuil/38fadc56-4e15-4be8-9b79-2659f09a17cd

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