FDA Warning Letter — Kevin R. Bender, M.D.

Case 680072 — FEI 3023815166

The FDA took a Warning Letter action against Kevin R. Bender, M.D. on May 2, 2024 (Tamarac, FL). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Kevin R. Bender, M.D.
Date
May 2, 2024
Fiscal Year
2024
Product Type
Drugs
Center
CDER
Location
Tamarac, FL (United States)