FDA Warning Letter — Medefil Incorporated

Case 97345 — FEI 3001677091

The FDA took a Warning Letter action against Medefil Incorporated on June 10, 2010 (Glendale Heights, IL). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Medefil Incorporated
Date
June 10, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Glendale Heights, IL (United States)