FDA Warning Letter — MRP, LLC

Case 46018 — FEI 1000151124

The FDA took a Warning Letter action against MRP, LLC on April 3, 2009 (Nashville, TN). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
MRP, LLC
Date
April 3, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Nashville, TN (United States)