# Eurofins Biopharma Product Testing, Denmark A/S, Glostrup, Denmark – FDA Inspections

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-denmark-as/b229d16c-8c5e-4288-9c41-ff6ea8ba3df5

> Inspection records and compliance data for Eurofins Biopharma Product Testing, Denmark A/S in Glostrup. 5 FDA inspections on record, last inspected May 17, 2023.

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## Details

- Name: Eurofins Biopharma Product Testing, Denmark A/S
- FEI Number: 3006272083
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: Ornebjergvej 1
- City: Glostrup
- Country Name: Denmark
- Address: Ornebjergvej 1, Glostrup, Denmark
- Country: Denmark

## Related Documents

- FDA Inspection 1222906 - Eurofins Biopharma Product Testing, Denmark A/S - 2023-05-17 — classification: No Action Indicated (NAI), source: FDA, date: May 17, 2023
- [FDA Inspection 976102 - Eurofins Biopharma Product Testing, Denmark A/S - 2016-06-22](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-denmark-as/aef8fe15-3be8-45e4-b1ad-0b861b1efd96) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 22, 2016
- FDA Inspection 811362 - Eurofins Biopharma Product Testing, Denmark A/S - 2012-12-14 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2012
- FDA Inspection 780431 - Eurofins Biopharma Product Testing, Denmark A/S - 2012-03-30 — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- FDA Inspection 578807 - Eurofins Biopharma Product Testing, Denmark A/S - 2009-05-12 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2009

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