FDA Warning Letter — Tubilux Pharma Spa

Case 523119 — FEI 3003854110

The FDA took a Warning Letter action against Tubilux Pharma Spa on July 6, 2017 (Pomezia, Italy). The action was issued by CDER and concerns drugs products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Tubilux Pharma Spa
Date
July 6, 2017
Fiscal Year
2017
Product Type
Drugs
Center
CDER
Location
Pomezia (Italy)