# MEDTRONIC IRELAND – FDA Inspection, Oct 27, 2016

Source: https://www.keypedia.com/records/fda_inspections/medtronic-ireland/e2cb75b8-7bab-4f74-b76f-d1438c51fe76
Source feed: FDA_Inspections

> FDA inspection 992239 of MEDTRONIC IRELAND, October 27, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 211. Form 483 issued. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 992239
- Company Name: MEDTRONIC IRELAND
- Inspection Date: 2016-10-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 969068 - 2016-02-12](https://www.keypedia.com/records/fda_inspections/medtronic-ireland/e6fb5200-e5cb-4ffd-b557-cab0ce7c95b1)
- FDA Inspection 904708 - 2014-11-20
- [FDA Inspection 880677 - 2014-05-15](https://www.keypedia.com/records/fda_inspections/medtronic-ireland/228a5a46-fd04-4073-a485-675f7dac6448)
- FDA Inspection 823591 - 2013-03-22
- FDA Inspection 789749 - 2012-06-28

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/medtronic-ireland/eb59435f-e3d7-493a-9b22-52e3575f021d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7