# FDA Inspection 1216203 - Lifeaire Systems - August 29, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/lifeaire-systems/c739801c-e272-4145-8b6d-54a02a42b174
Source feed: FDA_Inspections

> FDA Inspection 1216203 for Lifeaire Systems on August 29, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1216203
- Company Name: Lifeaire Systems
- Inspection Date: 2023-08-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1233169 - 2024-01-31](https://www.globalkeysolutions.net/records/fda_inspections/lifeaire-systems/f8c162b3-05c5-4847-9ef0-be95300c4eca)
- [FDA Inspection 1216203 - 2023-08-29](https://www.globalkeysolutions.net/records/fda_inspections/lifeaire-systems/d095f6ee-d70f-4307-b9a7-f68c5193d4ba)

Company: https://www.globalkeysolutions.net/companies/lifeaire-systems/4821728e-ad4a-44bf-8c6e-9b575ed25e65

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