FDA Warning Letter — Renaissance Lakewood, LLC

Case 291117 — FEI 2242829

The FDA took a Warning Letter action against Renaissance Lakewood, LLC on August 27, 2012 (Lakewood, NJ). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Renaissance Lakewood, LLC
Date
August 27, 2012
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Lakewood, NJ (United States)