FDA Warning Letter — Munroe Regional Medical Center Clinical Laboratory

Case 85364 — FEI 3006168886

The FDA took a Warning Letter action against Munroe Regional Medical Center Clinical Laboratory on Jan 11, 2010 (Ocala, FL). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Munroe Regional Medical Center Clinical Laboratory
Date
Jan 11, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Ocala, FL (United States)