# FDA 483 - Gobiquity, Inc - February 12, 2026

Source: https://www.globalkeysolutions.net/records/483/gobiquity-inc/7f306094-d880-4f6a-bf73-7f98bc531833

> FDA 483 for Gobiquity, Inc on February 12, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Gobiquity, Inc
- Inspection Date: 2026-02-12
- Product Type: device
- Office Name: New Orleans District Office
- Summary: An FDA inspection of Gobiquity, Inc. in Nashville, TN, revealed significant deficiencies in the firm's quality management system, particularly regarding the application of a risk-based approach. The inspection found inadequate controls over complaint handling, nonconforming product, corrective actions, data analysis, and design changes, especially concerning cybersecurity vulnerabilities. These issues led to product recalls and could adversely affect patient safety and data security.

## Related Documents

- [483 - 2023-06-15](https://www.globalkeysolutions.net/records/483/gobiquity-inc/6730c4a9-d5ab-45bc-9bc7-9e2901fb37de)

## Related Officers

- [Jamie P. Webb](https://www.globalkeysolutions.net/people/jamie-p-webb/9e052469-54f7-4d56-b977-27babbdac09b)

Company: https://www.globalkeysolutions.net/companies/gobiquity-inc/d3a6698c-d438-4e5b-a7cb-d10e8882eceb

Office: https://www.globalkeysolutions.net/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea