FDA Warning Letter — Hemofarm AD Vrsac

Case 278337 — FEI 3006082102

The FDA took a Warning Letter action against Hemofarm AD Vrsac on June 20, 2012 (Vrsac, Serbia). The action was issued by CDER and concerns drugs products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Hemofarm AD Vrsac
Date
June 20, 2012
Fiscal Year
2012
Product Type
Drugs
Center
CDER
Location
Vrsac (Serbia)