# FDA Inspection 801998 - Vyaire Medical - September 05, 2012

Source: https://www.keypedia.com/records/fda_inspections/vyaire-medical/4349dd01-cb61-4158-a86e-02b9e0873c90
Source feed: FDA_Inspections

> FDA Inspection 801998 for Vyaire Medical on September 05, 2012. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 801998
- Company Name: Vyaire Medical
- Inspection Date: 2012-09-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 899913 - 2014-09-30](https://www.keypedia.com/records/fda_inspections/vyaire-medical/826b6a34-a7b6-4ce5-a50e-09c647f6eb96)
- [FDA Inspection 754525 - 2011-11-25](https://www.keypedia.com/records/fda_inspections/vyaire-medical/d91ff697-7e08-4cb3-85c2-4ad52bdad4ca)
- [FDA Inspection 614960 - 2009-09-18](https://www.keypedia.com/records/fda_inspections/vyaire-medical/7ff6ab2f-9bdf-4fba-a284-40098ce0aca4)

Company: https://www.keypedia.com/companies/vyaire-medical/b262e1cf-6312-43e4-b883-b45ebc307a70

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