# 3D Diagnostix Inc. – FDA Inspection, Nov 21, 2025

Source: https://www.keypedia.com/records/fda_inspections/3d-diagnostix-inc/014e653c-c6e5-4fa9-a019-f1bad4a6714d
Source feed: FDA_Inspections

> FDA inspection 1292268 of 3D Diagnostix Inc., November 21, 2025. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1292268
- Company Name: 3D Diagnostix Inc.
- Inspection Date: 2025-11-21
- 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: New England District Office
- Citation Count: 8

## Related Officers

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

Company: https://www.keypedia.com/companies/3d-diagnostix-inc/6904bc5d-6c04-4b43-8887-3cdffe87aefb

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144