FDA Warning Letter — Cerovene Inc.

Case 72223 — FEI 3005890568

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

Action Details

Facility
Cerovene Inc.
Date
October 13, 2009
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Valley Cottage, NY (United States)