FDA Warning Letter — Viraban

Case 75564 — FEI 3007820942

The FDA took a Warning Letter action against Viraban on Sep 14, 2009 (Mandeville, LA). The action was issued by CDER and concerns drugs products.

Action Details

Facility
Viraban
Date
Sep 14, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Mandeville, LA (United States)