FDA inspection

ABBVIE IRELAND NL B.V. BALLYTIVNAN: FDA inspection ending Sep 10, 2024

FDA inspection 1281055 · Voluntary Action Indicated (VAI) · Sligo

Key facts

Inspection ID 1281055
Firm ABBVIE IRELAND NL B.V. BALLYTIVNAN
FEI number 3012441529
Address Ballytivnan
City Sligo
Fiscal year 2024
Inspection end date Sep 10, 2024
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
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

Browse all FDA inspections