# FDA Inspection 1255108 - SLEEPIZ AG - October 24, 2024

Source: https://www.keypedia.com/records/fda_inspections/sleepiz-ag/014f7d4a-151f-4629-b587-b73d1758589a
Source feed: FDA_Inspections

> FDA Inspection 1255108 for SLEEPIZ AG on October 24, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1255108
- Company Name: SLEEPIZ AG
- Inspection Date: 2024-10-24
- 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 1255108 - 2024-10-24](https://www.keypedia.com/records/fda_inspections/sleepiz-ag/9585bea6-c54c-428c-b1aa-7109568e97d3)
- [FDA Inspection 1255108 - 2024-10-24](https://www.keypedia.com/records/fda_inspections/sleepiz-ag/81d587a5-2f21-461f-ba0b-515999f73197)

Company: https://www.keypedia.com/companies/sleepiz-ag/7bf127ed-a46d-451b-bc55-b9c1882e5cb6

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