# FDA Inspection 1213001 - SLEEP 8 LLC - August 04, 2023

Source: https://www.keypedia.com/records/fda_inspections/sleep-8-llc/d525963b-8774-4a4c-a3d4-521b00b3fcff
Source feed: FDA_Inspections

> FDA Inspection 1213001 for SLEEP 8 LLC on August 04, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1213001
- Company Name: SLEEP 8 LLC
- Inspection Date: 2023-08-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1213001 - 2023-08-04](https://www.keypedia.com/records/fda_inspections/sleep-8-llc/806880d9-97e6-4a52-96d8-16b67c14cc73)

Company: https://www.keypedia.com/companies/sleep-8-llc/bf78abab-1b8d-4ae4-ae8c-16e15be62844

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