FDA inspection

Abbott GmbH: FDA inspection ending Sep 23, 2010

FDA inspection 684828 · Voluntary Action Indicated (VAI) · Wiesbaden

Key facts

Inspection ID 684828
Firm Abbott GmbH
FEI number 3002809144
Address Max-Planck-Ring 2
City Wiesbaden
Country Germany
Fiscal year 2010
Inspection end date Sep 23, 2010
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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