FDA inspection

Tubilux Pharma Spa: FDA inspection ending Jun 14, 2024

FDA inspection 1263915 · Voluntary Action Indicated (VAI) · Pomezia

Key facts

Inspection ID 1263915
Firm Tubilux Pharma Spa
FEI number 3003854110
Address Via Costarica 20/22
City Pomezia
Country Italy
Fiscal year 2024
Inspection end date Jun 14, 2024
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No 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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