# FDA 483 - Microtransponder Inc. - March 19, 2026

Source: https://www.keypedia.com/records/483/microtransponder-inc/e06bb4f8-f7a1-47cd-884a-8d879e85744a

> FDA 483 for Microtransponder Inc. on March 19, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Microtransponder Inc.
- Inspection Date: 2026-03-19
- Product Type: device
- Office Name: Dallas District Office
- Summary: An FDA inspection of MicroTransponder, Inc. in Lakeway, TX, revealed a failure to submit Medical Device Reports (MDRs) within the required 30-day timeframe. The firm did not report serious injuries, including patient loss of consciousness and seizures, associated with their marketed devices. This indicates a critical deficiency in their post-market surveillance and patient safety reporting procedures.

## Related Officers

- [Jacey Roy](https://www.keypedia.com/people/jacey-roy/6c4d5a32-4aa3-43b0-a06f-40757863219e)

Company: https://www.keypedia.com/companies/microtransponder-inc/b56d0db4-4ee3-4dd1-8d23-2b721855f1f5

Office: https://www.keypedia.com/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9