FDA inspection

Abbott Ireland: FDA inspection ending Mar 2, 2017

FDA inspection 1010736 · No Action Indicated (NAI) · Sligo

Key facts

Inspection ID 1010736
Firm Abbott Ireland
FEI number 3008344661
Address Diagnostics Division, Finisklin Road
City Sligo
Fiscal year 2017
Inspection end date Mar 2, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None 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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