# FDA Inspection 1122345 - Vertos Medical, Inc. - March 17, 2020

Source: https://www.keypedia.com/records/fda_inspections/vertos-medical-inc/3af458d4-9384-4fd5-861e-0a9fc3e83fff
Source feed: FDA_Inspections

> FDA Inspection 1122345 for Vertos Medical, Inc. on March 17, 2020. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1122345
- Company Name: Vertos Medical, Inc.
- Inspection Date: 2020-03-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1205079 - 2023-04-05](https://www.keypedia.com/records/fda_inspections/vertos-medical-inc/0bb7516e-46d3-4e55-9a14-96b4b7ecd393)
- [FDA Inspection 1205079 - 2023-04-05](https://www.keypedia.com/records/fda_inspections/vertos-medical-inc/d8debccb-dc6b-40f2-880f-4edb5448e14e)
- [FDA Inspection 1122345 - 2020-03-17](https://www.keypedia.com/records/fda_inspections/vertos-medical-inc/c712313d-2d7c-4994-be52-ac53b8203ebd)
- [FDA Inspection 992059 - 2016-11-10](https://www.keypedia.com/records/fda_inspections/vertos-medical-inc/bda96a38-3702-47e1-8122-492f28776e32)
- [FDA Inspection 992059 - 2016-11-10](https://www.keypedia.com/records/fda_inspections/vertos-medical-inc/af42a820-c59b-4881-8648-0e453b5c7e1c)

Company: https://www.keypedia.com/companies/vertos-medical-inc/82ed87b6-7fe4-46d7-ab8f-201a3980e2be

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