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483
•Steven Zeig, MD•March 16, 2015

Steven Zeig, MD – FDA 483, Mar 16, 2015

Record Details

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.

Company
Steven Zeig, MD
Inspection date
March 16, 2015
Product type
drugs
Office
Office of Medical Device and Radiological Health Division II
People
  • Ana P. Barido (investigator)
  • Angelica M. Chica
View Company Profile

ID · 7da32916-2d25-4724-824f-69118505634a

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