# FDA 483 - Brien E. Pierpont, M.D. - February 26, 2026

Source: https://www.keypedia.com/records/483/brien-e-pierpont-md/7497bae3-afaf-4730-832c-6a17739e4ec0

> FDA 483 for Brien E. Pierpont, M.D. on February 26, 2026. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Brien E. Pierpont, M.D.
- Inspection Date: 2026-02-26
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Advance Medical Research, Inc. in Saint Petersburg, FL, a clinical investigator, revealed significant deviations from the investigational plan. The firm failed to conduct investigations in accordance with the signed statement of investigator and investigational plan, leading to issues with subject eligibility, incorrect treatment stratification, and missing laboratory samples. These findings indicate a failure to adhere to study protocols and regulatory requirements.

## Related Officers

- [issuing_officer](https://www.keypedia.com/people/chinyere-a-asanya/5d417b03-0ebb-4903-9626-3528d9d95536)

Company: https://www.keypedia.com/companies/brien-e-pierpont-md/278c4473-96d2-46fc-abfd-6ebf66e51201

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