# FDA Inspection 1261790 - Vesper Medical, Inc. - February 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/vesper-medical-inc/2d9e6e05-0262-4a69-a473-ac853d8ea9a0
Source feed: FDA_Inspections

> FDA Inspection 1261790 for Vesper Medical, Inc. on February 19, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1261790
- Company Name: Vesper Medical, Inc.
- Inspection Date: 2025-02-19
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1227305 - 2024-01-08](https://www.keypedia.com/records/fda_inspections/vesper-medical-inc/dc1d3276-1c45-4743-a552-ae81a14a09d9)

Company: https://www.keypedia.com/companies/vesper-medical-inc/3f8034f1-c361-427a-bec4-5b84324b61ff

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