# Integra Lifesciences (Ireland) Limited, SRAGH Tullamore, Ireland – FDA Inspections

Source: https://www.keypedia.com/companies/integra-lifesciences-ireland-limited/9d1683e2-95a2-48b6-8943-295c852ba3ce

> Inspection records and compliance data for Integra Lifesciences (Ireland) Limited in SRAGH Tullamore. 5 FDA inspections on record, 1 Form 483, last inspected December 14, 2018.

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## Details

- Name: Integra Lifesciences (Ireland) Limited
- FEI Number: 3006697299
- Address Line 1: Tullamore Business & Technology Park, IDA BUSINESS and TECHNOLOGY PARK
- City: SRAGH Tullamore
- Country Name: Ireland
- Address: Tullamore Business & Technology Park, IDA BUSINESS and TECHNOLOGY PARK, SRAGH Tullamore, Ireland
- Country: Ireland

## Related Documents

- [FDA Inspection 1094949 - Integra Lifesciences (Ireland) Limited - 2018-12-14](https://www.keypedia.com/records/fda_inspections/integra-lifesciences-ireland-limited/3cb18e3d-4ea0-462a-9f30-727c09bc37ba) — source: FDA, date: December 14, 2018
- FDA Inspection 1072147 - Integra Lifesciences (Ireland) Limited - 2018-04-26 — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2018
- FDA Inspection 1072147 - Integra Lifesciences (Ireland) Limited - 2018-04-26 — classification: No Action Indicated (NAI), source: FDA, date: April 26, 2018
- FDA Inspection 919158 - Integra Lifesciences (Ireland) Limited - 2015-03-05 — classification: No Action Indicated (NAI), source: FDA, date: March 5, 2015
- FDA Inspection 799848 - Integra Lifesciences (Ireland) Limited - 2012-08-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 23, 2012
- FDA Inspection 799848 - Integra Lifesciences (Ireland) Limited - 2012-08-23 — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2012
- [FDA Inspection 694696 - Integra Lifesciences (Ireland) Limited - 2010-09-30](https://www.keypedia.com/records/fda_inspections/integra-lifesciences-ireland-limited/919d415b-f6b1-40bb-8c6e-bbcd3398f276) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2010

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