# FDA Inspection 1195082 - Sleep Joy International LLC - January 20, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/sleep-joy-international-llc/3a15346b-5c92-4953-8ce1-5541398cf758
Source feed: FDA_Inspections

> FDA Inspection 1195082 for Sleep Joy International LLC on January 20, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1195082
- Company Name: Sleep Joy International LLC
- Inspection Date: 2023-01-20
- 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 1195082 - 2023-01-20](https://www.globalkeysolutions.net/records/fda_inspections/sleep-joy-international-llc/a7361d77-19f8-4888-a244-79d7b8a54890)
- [FDA Inspection 1021730 - 2017-08-04](https://www.globalkeysolutions.net/records/fda_inspections/sleep-joy-international-llc/741aa312-0503-4b4f-b69b-c84f16901d6a)
- [FDA Inspection 822531 - 2013-03-12](https://www.globalkeysolutions.net/records/fda_inspections/sleep-joy-international-llc/847fab62-0df8-4d70-8f08-7a45be504148)

Company: https://www.globalkeysolutions.net/companies/sleep-joy-international-llc/883656db-56f0-406c-b403-37d5ef54cdde

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