FDA Warning Letter — Trifarma S.p.A.

Case 424161 — FEI 3002807260

The FDA took a Warning Letter action against Trifarma S.p.A. on July 7, 2014 (Rozzano, Italy). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Trifarma S.p.A.
Date
July 7, 2014
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Rozzano (Italy)