# FDA Inspection 1222917 - Xenios Ag - October 19, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/xenios-ag/de79d13c-d557-4200-8fbd-76c83852c378
Source feed: FDA_Inspections

> FDA Inspection 1222917 for Xenios Ag on October 19, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1222917
- Company Name: Xenios Ag
- Inspection Date: 2023-10-19
- 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 1222917 - 2023-10-19](https://www.globalkeysolutions.net/records/fda_inspections/xenios-ag/78238465-179b-40cc-84a6-498d5c09982d)

Company: https://www.globalkeysolutions.net/companies/xenios-ag/ea2f0cd9-ac7d-490d-bb74-a7e515f9796d

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