# FDA Inspection 1180862 - NUVOAIR AB - September 22, 2022

Source: https://www.keypedia.com/records/fda_inspections/nuvoair-ab/d0bade01-4b7c-4a0f-bb20-673d88304670
Source feed: FDA_Inspections

> FDA Inspection 1180862 for NUVOAIR AB on September 22, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180862
- Company Name: NUVOAIR AB
- Inspection Date: 2022-09-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1180862 - 2022-09-22](https://www.keypedia.com/records/fda_inspections/nuvoair-ab/23e52432-e8e9-4079-b162-130319c65cc3)

Company: https://www.keypedia.com/companies/nuvoair-ab/249f1a45-4e92-4418-b938-7ce5ac1dc9da

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