FDA inspection

Tubilux Pharma Spa: FDA inspection ending Dec 9, 2016

FDA inspection 998341 · Official Action Indicated (OAI) · Pomezia

Key facts

Inspection ID 998341
Firm Tubilux Pharma Spa
FEI number 3003854110
Address Via Costarica 20/22
City Pomezia
Country Italy
Fiscal year 2017
Inspection end date Dec 9, 2016
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs
Warning letter 523119

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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