# FDA 483 - Lawrence Ginsberg, M.D. - July 29, 2025

Source: https://www.globalkeysolutions.net/records/483/lawrence-ginsberg-md/f212a243-ab8b-4617-b026-fc2a14195fe4

> FDA 483 for Lawrence Ginsberg, M.D. on July 29, 2025. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Lawrence Ginsberg, M.D.
- Inspection Date: 2025-07-29
- Product Type: drugs
- Office Name: Dallas District Office
- Summary: An FDA inspection of Lawrence Ginsberg, M.D. in Houston, TX, a clinical investigator, revealed that investigations were not conducted in accordance with the signed statement of investigator and investigational plan. The firm failed to ensure contemporaneous documentation of subject eligibility decisions and proper attribution of screening assessments. These findings indicate significant deficiencies in record-keeping and adherence to study protocols.

## Related Officers

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

Company: https://www.globalkeysolutions.net/companies/lawrence-ginsberg-md/9aed9b52-fb82-48a6-a033-7ce8397ff001

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