# FDA Inspection 1080947 - SleepMe Inc - December 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/sleepme-inc/9c9d8a9c-2f11-4d36-b163-f3db93bcdb8c
Source feed: FDA_Inspections

> FDA Inspection 1080947 for SleepMe Inc on December 12, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1080947
- Company Name: SleepMe Inc
- Inspection Date: 2018-12-12
- 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 1080947 - 2018-12-12](https://www.globalkeysolutions.net/records/fda_inspections/sleepme-inc/23dd6dd0-028b-4e50-a539-3afad7f36605)

Company: https://www.globalkeysolutions.net/companies/sleepme-inc/8f46a515-6446-4ab5-9aa5-d63b65df1ec2

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