# FDA 483 - Beasley E. Robert, MD - July 21, 2025

Source: https://www.keypedia.com/records/483/beasley-e-robert-md/0c7246a5-d19d-438d-b091-bf607bbe719e

> FDA 483 for Beasley E. Robert, MD on July 21, 2025. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Beasley E. Robert, MD
- Inspection Date: 2025-07-21
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: Robert E. Beasley, MD, a clinical investigator in Fort Lauderdale, FL, was cited for failing to conduct an investigation according to the investigational plan. The inspection revealed significant delays in reporting serious adverse events (SAEs) to the sponsor. Multiple SAEs were reported months, and in some cases over a year, after the firm became aware of them.

## Related Documents

- [483 - 2025-07-21](https://www.keypedia.com/records/483/beasley-e-robert-md/d1d9875a-7f78-42c4-9d7d-2ad4faa582db)

## Related Officers

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

Company: https://www.keypedia.com/companies/beasley-e-robert-md/7386c4fc-5adc-4a2c-943b-2db515aeb07d

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