# FDA 483 - Josefina Tur, MD - July 29, 2019

Source: https://www.keypedia.com/records/483/josefina-tur-md/01a53e6c-3b23-48d8-b9a7-91e62dbe6187

> FDA 483 for Josefina Tur, MD on July 29, 2019. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Josefina Tur, MD
- Inspection Date: 2019-07-29
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Josefina Tur, MD, a clinical investigator in Miami, FL, identified one observation. The firm failed to conduct an investigation in accordance with the signed statement of investigator and investigational plan. This involved not collecting required patient assessments and blood chemistry laboratories as specified in the protocol.

## Related Officers

- [Richard A. Lyght](https://www.keypedia.com/people/richard-a-lyght/8d60b5c0-4acd-4abc-979a-fb4b3e82964d)

Company: https://www.keypedia.com/companies/josefina-tur-md/b7ed07d0-fad1-4483-9120-bb18bae1c6aa

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