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483
•Suresh Anne, M.D.•February 13, 2026

Suresh Anne, M.D. – FDA 483, Feb 13, 2026

Record Details

An FDA inspection of Suresh Anne, M.D., a clinical investigator in Flint, MI, revealed significant deviations from investigational plans and protocols. The firm failed to enroll eligible subjects and did not follow required safety monitoring procedures for investigational products. Additionally, the investigator did not promptly report non-serious adverse events to the sponsor as required by the study protocol.

Company
Suresh Anne, M.D.
Inspection date
February 13, 2026
Product type
drugs
Office
Division of Pharmaceutical Quality Operations III
People
  • Dina A. Tallman (investigator)
  • Victoria R. Flournoy
View Company Profile

ID · 42c11be6-f2e0-4338-920b-39468eb38f62

Other documents for Suresh Anne, M.D.
  • 483 - 2023-05-19May 19, 2023

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