FDA Warning Letter — Stuart A. Harlin, MD

Case 117891 — FEI 3008266152

The FDA took a Warning Letter action against Stuart A. Harlin, MD on July 21, 2010 (Pensacola, FL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Stuart A. Harlin, MD
Date
July 21, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Pensacola, FL (United States)