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483
•Wendy C. Daly, M.D.•July 1, 2019

Wendy C. Daly, M.D. – FDA 483, Jul 1, 2019

Record Details

An FDA inspection of Wendy C. Daly, M.D. in Louisville, KY, a clinical investigator, revealed significant issues in clinical trial conduct. Observations included the failure to report adverse events to the sponsor and the lack of accurate and complete case histories, with discrepancies between source documents and electronic case report forms.

Company
Wendy C. Daly, M.D.
Inspection date
July 1, 2019
Product type
drugs
Office
Cincinnati District Office
Person
  • Karen M. Cooper (investigator)
View Company Profile

ID · 1aa602af-ac2b-44fa-988a-93356d271a12

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