FDA Warning Letter — Kanec Usa, Inc.

Case 120868 — FEI 1000526329

The FDA took a Warning Letter action against Kanec Usa, Inc. on October 8, 2010 (Miramar, FL). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Kanec Usa, Inc.
Date
October 8, 2010
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
Miramar, FL (United States)