# ZIOSOFT, INC. – FDA Inspection, Dec 18, 2025

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

> FDA inspection 1296688 of ZIOSOFT, INC., December 18, 2025. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 4

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sunita-pandey/008e5bb8-0eb3-45d8-8524-734ac0454250)

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