# INFLAMMATIX INC – FDA 483, Apr 30, 2026

Source: https://www.keypedia.com/records/483/inflammatix-inc/e30d800c-942c-4c0a-8efd-6d1f9e52db02

> FDA 483 for INFLAMMATIX INC on April 30, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: INFLAMMATIX INC
- Inspection Date: 2026-04-30
- Product Type: device
- Office Name: Division of Human and Animal Food Operations - West V
- Summary: An FDA inspection of INFLAMMATIX INC in Sunnyvale, CA, identified a single observation related to regulatory compliance for medical devices. The firm failed to provide correct unique device identifier (UDI) information to the Global Unique Device Identification Database (GUDID) for its Myma and Triverity devices. This lapse occurred prior to the commercial distribution of these devices, indicating a significant regulatory oversight.

## Related Officers

- [Brittany D. Mccracken](https://www.keypedia.com/people/brittany-d-mccracken/a869ecee-3b7b-4c1a-8c77-7efb1a3d902a)

Company: https://www.keypedia.com/companies/inflammatix-inc/3b2df7fc-968c-40e2-b0c5-bdc1a242e461

Office: https://www.keypedia.com/offices/division-of-human-and-animal-food-operations-west-v/0f4dd01e-8e8a-4336-9abe-ce8b3d309e8b