# FDA Inspection 1046153 - Vivorte, Inc. - March 02, 2018

Source: https://www.keypedia.com/records/fda_inspections/vivorte-inc/c4e6e2d8-40e5-40fc-89bc-40d09cfa3a69
Source feed: FDA_Inspections

> FDA Inspection 1046153 for Vivorte, Inc. on March 02, 2018. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1046153
- Company Name: Vivorte, Inc.
- Inspection Date: 2018-03-02
- 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 1157349 - 2021-11-23](https://www.keypedia.com/records/fda_inspections/vivorte-inc/7ce1bb3f-285a-47a1-ac6e-c30a9424c081)
- [FDA Inspection 1157349 - 2021-11-23](https://www.keypedia.com/records/fda_inspections/vivorte-inc/6fc55bde-7f68-441d-9fff-c9c9141c1447)
- [FDA Inspection 1046153 - 2018-03-02](https://www.keypedia.com/records/fda_inspections/vivorte-inc/85bd450b-9f43-48fb-b925-aa1d57e5c9de)
- [FDA Inspection 907928 - 2014-12-16](https://www.keypedia.com/records/fda_inspections/vivorte-inc/e6c893fa-ceb4-4638-94e2-14c46cac6403)

Company: https://www.keypedia.com/companies/vivorte-inc/3c7f2fbe-cc5b-442c-8c9f-2c95f314fb08

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