# FDA Inspection 1096539 - Breathe E-Z Systems, Inc. - July 17, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/breathe-e-z-systems-inc/7c50abff-e3ee-46a0-98ef-52d1a3529c9e
Source feed: FDA_Inspections

> FDA Inspection 1096539 for Breathe E-Z Systems, Inc. on July 17, 2019. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1096539
- Company Name: Breathe E-Z Systems, Inc.
- Inspection Date: 2019-07-17
- 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 1206550 - 2023-05-22](https://www.globalkeysolutions.net/records/fda_inspections/breathe-e-z-systems-inc/00676195-3d29-4f70-b298-e045d44e291c)
- [FDA Inspection 1206550 - 2023-05-22](https://www.globalkeysolutions.net/records/fda_inspections/breathe-e-z-systems-inc/4726a9c4-bff0-4b3e-9ed5-8ae062307d7a)
- [FDA Inspection 1096539 - 2019-07-17](https://www.globalkeysolutions.net/records/fda_inspections/breathe-e-z-systems-inc/aa859cf8-f704-44df-8c2d-a8d48e049920)
- [FDA Inspection 807476 - 2012-11-07](https://www.globalkeysolutions.net/records/fda_inspections/breathe-e-z-systems-inc/90e6fb04-c2aa-46e6-9c38-ded506d5a260)
- [FDA Inspection 590070 - 2009-06-18](https://www.globalkeysolutions.net/records/fda_inspections/breathe-e-z-systems-inc/984ec607-e01c-4d8d-988e-bedd5fe4897d)

Company: https://www.globalkeysolutions.net/companies/breathe-e-z-systems-inc/1e53cae8-29f4-4357-a67e-7c4c6e508252

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