FDA inspection

AbbVie Deutschland GmbH & Co. KG: FDA inspection ending May 15, 2009

FDA inspection 584391 · Voluntary Action Indicated (VAI) · Ludwigshafen

Key facts

Inspection ID 584391
Firm AbbVie Deutschland GmbH & Co. KG
FEI number 3002807401
Address Knollstrasse
City Ludwigshafen
Country Germany
Fiscal year 2009
Inspection end date May 15, 2009
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
  • 10–99 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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