FDA Warning Letter — Biovation Labs

Case 118988 — FEI 1000220648

The FDA took a Warning Letter action against Biovation Labs on December 28, 2010 (West Valley City, UT). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Biovation Labs
Date
December 28, 2010
Fiscal Year
2011
Product Type
Drugs
Center
CDER
Location
West Valley City, UT (United States)