# FDA 483 - Steven (NMI) Zeig, MD - March 16, 2015

Source: https://www.globalkeysolutions.net/records/483/steven-nmi-zeig-md/7da32916-2d25-4724-824f-69118505634a

> FDA 483 for Steven (NMI) Zeig, MD on March 16, 2015. Product: drugs. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Steven (NMI) Zeig, MD
- Inspection Date: 2015-03-16
- Product Type: drugs
- Office Name: Office of Medical Device and Radiological Health Division II
- Summary: An FDA inspection of Steven Zeig, M.D., Clinical Investigator, revealed significant deviations from the investigational plan and protocol. Observations included the enrollment of subjects who met exclusion criteria without proper waivers and the administration of study drug by unauthorized personnel. These findings indicate a lack of adherence to study protocols and proper oversight in clinical investigations.

## Related Officers

- [Angelica M. Chica, Investigator](https://www.globalkeysolutions.net/people/angelica-m-chica-investigator/51e64d31-9f43-462b-bd8d-80cb977d91e0)
- [Ana R. Barido, Investigator](https://www.globalkeysolutions.net/people/ana-r-barido-investigator/386462f2-a036-4b2d-b263-4990f5153890)

Company: https://www.globalkeysolutions.net/companies/steven-nmi-zeig-md/6b24b953-a3eb-4cec-b740-e10205c289dc

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