FDA Warning Letter — Martin K. Dineen, M.D.

Case 43661 — FEI 3003576224

The FDA took a Warning Letter action against Martin K. Dineen, M.D. on Dec 22, 2008 (Daytona Beach, FL). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Martin K. Dineen, M.D.
Date
Dec 22, 2008
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Daytona Beach, FL (United States)