FDA Warning Letter — Synthexim

Case 434927 — FEI 3002806640

The FDA took a Warning Letter action against Synthexim on Jul 18, 2014 (Calais, France). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Synthexim
Date
Jul 18, 2014
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Calais (France)