# FDA Inspection 1296688 - ZIOSOFT, INC. - December 18, 2025

Source: https://www.keypedia.com/records/fda_inspections/ziosoft-inc/ef5f8b82-1a89-4df9-9429-0e374cd1180a
Source feed: FDA_Inspections

> FDA Inspection 1296688 for ZIOSOFT, INC. on December 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1296688
- Company Name: ZIOSOFT, INC.
- Inspection Date: 2025-12-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations

## Related Documents

- [FDA Inspection 1296688 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/ziosoft-inc/1d03f16d-2b26-454b-a1b5-7268c60f1be2)
- [FDA Inspection 1296688 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/ziosoft-inc/b05dac23-8b6f-4589-815d-baea06422074)
- [FDA Inspection 1296688 - 2025-12-18](https://www.keypedia.com/records/fda_inspections/ziosoft-inc/0cce9185-0a5b-4fc4-8266-0078406be867)

Company: https://www.keypedia.com/companies/ziosoft-inc/99358037-f234-4a17-b716-582eb7884cf2

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8