# Eurofins Biopharma Product Testing Ireland Limited, Dungarvan, Ireland – FDA Inspections

Source: https://www.keypedia.com/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. 6 FDA inspections on record, last inspected June 20, 2025.

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## Details

- Name: Eurofins Biopharma Product Testing Ireland Limited
- FEI Number: 3002807550
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: Ida Industrial Estate
- City: Dungarvan
- Country Name: Ireland
- Address: Ida Industrial Estate, Dungarvan, Ireland
- Country: Ireland

## Related Documents

- FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - 2025-06-20 — source: FDA, date: June 20, 2025
- FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - 2025-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- FDA Inspection 1280309 - Eurofins Biopharma Product Testing Ireland Limited - 2025-06-20 — classification: No Action Indicated (NAI), source: FDA, date: June 20, 2025
- FDA Inspection 1270954 - Eurofins Biopharma Product Testing Ireland Limited - 2023-05-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 26, 2023
- FDA Inspection 1127573 - Eurofins Biopharma Product Testing Ireland Limited - 2019-01-17 — source: FDA, date: January 17, 2019
- FDA Inspection 1008821 - Eurofins Biopharma Product Testing Ireland Limited - 2017-02-24 — classification: No Action Indicated (NAI), source: FDA, date: February 24, 2017
- FDA Inspection 826551 - Eurofins Biopharma Product Testing Ireland Limited - 2013-03-29 — classification: No Action Indicated (NAI), source: FDA, date: March 29, 2013
- FDA Inspection 618581 - Eurofins Biopharma Product Testing Ireland Limited - 2009-09-30 — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2009

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