FDA Warning Letter — Bioniche Pharma Group

Case 70843 — FEI 3007210540

The FDA took a Warning Letter action against Bioniche Pharma Group on Sep 14, 2009 (Lake Forest, IL). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Bioniche Pharma Group
Date
Sep 14, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Lake Forest, IL (United States)