# FDA 483 - Maria Cuesta Torres, M.D. - May 18, 2023

Source: https://www.keypedia.com/records/483/maria-cuesta-torres-md/1ad88d2c-8141-44d2-8be9-a9e8eb64076b

> FDA 483 for Maria Cuesta Torres, M.D. on May 18, 2023. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Maria Cuesta Torres, M.D.
- Inspection Date: 2023-05-18
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Maria Cuesta Torres, M.D., a clinical investigator in Miami Lakes, FL, revealed a significant failure to maintain adequate and accurate case histories. Specifically, the firm lacked source documentation to support inclusion criteria for multiple subjects and failed to document changes made during subsequent evaluations. This indicates a serious deficiency in record-keeping practices for clinical investigations.

## Related Officers

- [investigator](https://www.keypedia.com/people/emily-a-baldwin/92d70174-7029-44f4-af30-e3230d4e9507)

Company: https://www.keypedia.com/companies/maria-cuesta-torres-md/becb7f83-cb86-422b-a4e0-c0fc53f62dc6

Office: https://www.keypedia.com/offices/office-of-medical-device-and-radiological-health-division-ii/ae9bd439-479a-420d-9dd8-9fe1fc0863d6