FDA inspection

Abbott GmbH: FDA inspection ending Feb 9, 2012

FDA inspection 770439 · No Action Indicated (NAI) · Wiesbaden

Key facts

Inspection ID 770439
Firm Abbott GmbH
FEI number 3002809144
Address Max-Planck-Ring 2
City Wiesbaden
Country Germany
Fiscal year 2012
Inspection end date Feb 9, 2012
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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