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TUBILUX PHARMA SPA — FDA Facility Profile

FEI 3003854110

TUBILUX PHARMA SPA is an FDA-registered facility (FEI 3003854110) located in POMEZIA, IT. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK. RegDataLab tracks 4 FDA inspections and 1 compliance action at this facility.

Facility Details

Location
POMEZIA (IT)
Registration Expires
December 31, 2026
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK
Source
decrs

Recent inspections

  • 1263915 (VAI Fri Jun 14 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1115090 (VAI Tue Dec 10 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1047718 (OAI Fri Apr 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998341 (OAI Fri Dec 09 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Import refusals

  • AEK-0517994-7/1/1 (Fri Feb 13 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)
  • AEK-6410552-7/1/1 (Wed Sep 15 2004 00:00:00 GMT+0000 (Coordinated Universal Time) — Drugs and Biologics)

FDA data resources