# DEPUY (IRELAND), Co. Cork, Ireland – FDA Inspections

Source: https://www.keypedia.com/companies/depuy-ireland/b2d65a16-dd39-44d5-af2b-d81e3933e10e

> Inspection records and compliance data for DEPUY (IRELAND) in Co. Cork. 5 FDA inspections on record, 1 Form 483, last inspected July 04, 2024.

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## Details

- Name: DEPUY (IRELAND)
- FEI Number: 3002854251
- Address Line 1: Loughbeg, Ringaskiddy
- City: Co. Cork
- Country Name: Ireland
- Address: Loughbeg, Ringaskiddy, Co. Cork, Ireland
- Country: Ireland

## Related Documents

- FDA Inspection 1245506 - DEPUY (IRELAND) - 2024-07-04 — classification: No Action Indicated (NAI), source: FDA, date: July 4, 2024
- FDA Inspection 1245506 - DEPUY (IRELAND) - 2024-07-04 — classification: No Action Indicated (NAI), source: FDA, date: July 4, 2024
- [483 - DEPUY (IRELAND) - 2016-12-09](https://www.keypedia.com/records/483/depuy-ireland/863653cd-e260-4c37-8594-7d47da63e20f) — source: FDA, date: December 9, 2016
- FDA Inspection 1002434 - DEPUY (IRELAND) - 2016-12-09 — source: FDA, date: December 9, 2016
- [FDA Inspection 1002434 - DEPUY (IRELAND) - 2016-12-09](https://www.keypedia.com/records/fda_inspections/depuy-ireland/db421f5c-1136-43c0-b34c-8b6805301aa2) — source: FDA, date: December 9, 2016
- FDA Inspection 1002434 - DEPUY (IRELAND) - 2016-12-09 — source: FDA, date: December 9, 2016
- FDA Inspection 912066 - DEPUY (IRELAND) - 2015-01-08 — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2015
- FDA Inspection 912066 - DEPUY (IRELAND) - 2015-01-08 — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2015
- FDA Inspection 772964 - DEPUY (IRELAND) - 2012-01-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2012
- [FDA Inspection 772964 - DEPUY (IRELAND) - 2012-01-26](https://www.keypedia.com/records/fda_inspections/depuy-ireland/e37e9ccd-f014-4aa4-b7a8-b94da282b02c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 26, 2012
- FDA Inspection 712736 - DEPUY (IRELAND) - 2011-02-03 — classification: No Action Indicated (NAI), source: FDA, date: February 3, 2011

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