# Eurofins Biopharma Product Testing Ireland Limited - Inspection Records

Source: https://www.globalkeysolutions.net/companies/eurofins-biopharma-product-testing-ireland-limited/2cded381-226c-436d-b95e-6f1b70b922d2

> Inspection records and compliance data for Eurofins Biopharma Product Testing Ireland Limited in Dungarvan, None. Access full analysis and detailed observations.

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## Details

- Name: Eurofins Biopharma Product Testing Ireland Limited
- FEI Number: 3002807550
- City: Dungarvan
- State: None
- Country Name: Ireland
- Address Line 1: Ida Industrial Estate
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - 2025-06-20](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/b5a5f352-2caa-41a6-9648-3cf3e17a1fb4) — source: FDA, date: June 20, 2025
- [FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - 2025-06-20](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/85fbc605-0972-4295-919d-4e91789b7fbb) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- [FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - 2025-06-20](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/d834f021-236c-4005-a28f-ca4dfc3bd67b) — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- [FDA Inspection 1270954 - Eurofins Biopharma Product Testing Ireland Limited - 2023-05-26](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/de6f5a0e-d3e9-4a64-a2b4-e5f938b251fa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2023
- [FDA Inspection 1008821 - Eurofins Biopharma Product Testing Ireland Limited - 2017-02-24](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/8470fa32-888d-4e85-be16-9e50d5047442) — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2017
- [FDA Inspection 826551 - Eurofins Biopharma Product Testing Ireland Limited - 2013-03-29](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/e5bd4b8f-5bb6-4e4e-ad38-35e24505d475) — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2013
- [FDA Inspection 618581 - Eurofins Biopharma Product Testing Ireland Limited - 2009-09-30](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-ireland-limited/a0911029-491a-463c-800d-0a5b59533e19) — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2009

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