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FDA Inspection
•MEDTRONIC IRELAND•May 15, 2014

MEDTRONIC IRELAND – FDA Inspection, May 15, 2014

Record Details

This FDA Inspection record concerns MEDTRONIC IRELAND, with an inspection on May 15, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
MEDTRONIC IRELAND
Inspection Date
May 15, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 228a5a46-fd04-4073-a485-675f7dac6448

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
880677
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of MEDTRONIC IRELAND

7
DateClassificationOfficeProject area
October 27, 2016VAICenter for Devices and Radiological HealthProject Evaluation: Devices
February 12, 2016VAICenter for Devices and Radiological HealthBioresearch Monitoring
November 20, 2014VAICenter for Devices and Radiological HealthBioresearch Monitoring
March 22, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
June 28, 2012NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 7 other inspections on the company page
Other documents for MEDTRONIC IRELAND
  • FDA Inspection 992239 - 2016-10-27
  • FDA Inspection 969068 - 2016-02-12
  • FDA Inspection 904708 - 2014-11-20
  • FDA Inspection 823591 - 2013-03-22
  • FDA Inspection 789749 - 2012-06-28

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