FDA inspection

Utah Medical Products Ltd: FDA inspection ending Apr 30, 2015

FDA inspection 928809 · Voluntary Action Indicated (VAI) · Athlone Leinster

Key facts

Inspection ID 928809
Firm Utah Medical Products Ltd
FEI number 3003105967
Address Athlone Business And Technology Park
City Athlone Leinster
Country Ireland
Fiscal year 2015
Inspection end date Apr 30, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

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

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