FDA Warning Letter — Larken Laboratories, Inc.

Case 71163 — FEI 3005966786

The FDA took a Warning Letter action against Larken Laboratories, Inc. on November 13, 2009 (Canton, MS). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Larken Laboratories, Inc.
Date
November 13, 2009
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Canton, MS (United States)