FDA Warning Letter — R4 LLC

Case 56802 — FEI 3006790946

The FDA took a Warning Letter action against R4 LLC on May 11, 2009 (Strongsville, OH). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
R4 LLC
Date
May 11, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Strongsville, OH (United States)