# FDA Inspection 1283424 - VirtuSense Technologies, Inc. - September 18, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/virtusense-technologies-inc/35f5b0a1-3c6f-45a5-8ea5-1654a1851f1c
Source feed: FDA_Inspections

> FDA Inspection 1283424 for VirtuSense Technologies, Inc. on September 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1283424
- Company Name: VirtuSense Technologies, Inc.
- Inspection Date: 2025-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1283424 - 2025-09-18](https://www.globalkeysolutions.net/records/fda_inspections/virtusense-technologies-inc/8de85e15-7a4f-4584-b3ec-6cafe5f04cbe)
- [FDA Inspection 1283424 - 2025-09-18](https://www.globalkeysolutions.net/records/fda_inspections/virtusense-technologies-inc/76871814-0152-4989-9273-c050bff6c9e9)
- [FDA Inspection 1283424 - 2025-09-18](https://www.globalkeysolutions.net/records/fda_inspections/virtusense-technologies-inc/f24dca6a-4a8b-4ca4-8eb4-542b0ccc4225)

Company: https://www.globalkeysolutions.net/companies/virtusense-technologies-inc/b3db6d8c-5486-4878-b041-e385ebbca4dc

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