FDA Warning Letter — Konec Inc.

Case 73603 — FEI 3000207081

The FDA took a Warning Letter action against Konec Inc. on Mar 16, 2010 (Tucson, AZ). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Konec Inc.
Date
Mar 16, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Tucson, AZ (United States)