# FDA 483 - Francisco Lopez Godoy, MD - October 27, 2025

Source: https://www.globalkeysolutions.net/records/483/francisco-lopez-godoy-md/e77081b8-455f-4f34-b8b0-6877fb9a2083

> FDA 483 for Francisco Lopez Godoy, MD on October 27, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Francisco Lopez Godoy, MD
- Inspection Date: 2025-10-27
- Product Type: device
- Office Name: Dallas District Office
- Summary: Panamericana Family Medicine Clinic in Houston, TX, was inspected regarding a non-significant risk device study. The inspection revealed that the clinical investigation did not meet abbreviated requirements for investigational device exemptions. Specifically, the firm failed to maintain adequate informed consent documents and ensure proper documentation of the informed consent process for study subjects.

## Related Officers

- [Ruth E. Medcalf](https://www.globalkeysolutions.net/people/ruth-e-medcalf/71a61d32-807b-4b73-9ea7-b59287e14e56)

Company: https://www.globalkeysolutions.net/companies/francisco-lopez-godoy-md/df9ec06d-c6d0-422c-90e4-6174589967ec

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