# FDA Inspection 1181772 - Medivis, Inc. - October 17, 2022

Source: https://www.keypedia.com/records/fda_inspections/medivis-inc/1df0858f-c1ac-412e-8d7e-aea2b2701fcc
Source feed: FDA_Inspections

> FDA Inspection 1181772 for Medivis, Inc. on October 17, 2022. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1181772
- Company Name: Medivis, Inc.
- Inspection Date: 2022-10-17
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1307926 - 2026-03-03](https://www.keypedia.com/records/fda_inspections/medivis-inc/001760f4-aa90-415d-b6a1-b69f8316f91e)
- [FDA Inspection 1307926 - 2026-03-03](https://www.keypedia.com/records/fda_inspections/medivis-inc/17f9300a-ec64-45ce-8102-33c427b570dc)
- [FDA Inspection 1181772 - 2022-10-17](https://www.keypedia.com/records/fda_inspections/medivis-inc/7206ba77-4487-4664-9b52-81aaa4d02e23)
- [FDA Inspection 1181772 - 2022-10-17](https://www.keypedia.com/records/fda_inspections/medivis-inc/0669e921-8898-4553-96a6-2ade884534a2)

Company: https://www.keypedia.com/companies/medivis-inc/15c971c0-2c88-457c-b8bc-00c4279a3d7b

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