# FDA 483 - Jose Carlos Lopez Escobar, M.D. - July 03, 2024

Source: https://www.keypedia.com/records/483/jose-carlos-lopez-escobar-md/b1f617f1-ac81-46f4-8c66-fab2347d72ad

> FDA 483 for Jose Carlos Lopez Escobar, M.D. on July 03, 2024. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Jose Carlos Lopez Escobar, M.D.
- Inspection Date: 2024-07-03
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Jose Carlos Lopez Escobar, M.D., operating as Health Care Family Rehab And Research Center in Hialeah, FL, identified a significant deficiency in clinical trial record-keeping. The firm failed to prepare or maintain adequate case histories for enrolled subjects. Specifically, five out of seven reviewed subjects lacked documentation confirming they met the inclusion criteria for prior Alzheimer's disease treatment.

## Related Documents

- [EIR - 2024-07-03](https://www.keypedia.com/records/eir/jose-carlos-lopez-escobar-md/ce246659-0bea-496e-91ca-e25ef4fa4287)

## Related Officers

- [Chantae D. Mitchell](https://www.keypedia.com/people/chantae-d-mitchell/0da68244-86f3-4119-b965-0b2dceb1c523)

Company: https://www.keypedia.com/companies/jose-carlos-lopez-escobar-md/1ab73ba5-d44c-4d0d-a02b-75503dce0910

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