FDA Warning Letter — Genus Lifesciences Inc.

Case 72043 — FEI 3003851100

The FDA took a Warning Letter action against Genus Lifesciences Inc. on October 13, 2009 (Allentown, PA). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Genus Lifesciences Inc.
Date
October 13, 2009
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Allentown, PA (United States)