# Eurofins Biopharma Product Testing, Denmark A/S - Inspection Records

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, None. Access full analysis and detailed observations.

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## Details

- Name: Eurofins Biopharma Product Testing, Denmark A/S
- FEI Number: 3006272083
- City: Glostrup
- State: None
- Country Name: Denmark
- Address Line 1: Ornebjergvej 1
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1222906 - Eurofins Biopharma Product Testing, Denmark A/S - 2023-05-17](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-denmark-as/1f9eb078-a863-4e62-a0d3-885a98f42d1e) — 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](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-denmark-as/3e5fbd89-11d6-423d-b6c5-e6ee994700f0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 14, 2012
- [FDA Inspection 780431 - Eurofins Biopharma Product Testing, Denmark A/S - 2012-03-30](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-denmark-as/d24ecae5-d799-4704-89d0-2ce78b4c9e23) — classification: No Action Indicated (NAI), source: FDA, date: March 30, 2012
- [FDA Inspection 578807 - Eurofins Biopharma Product Testing, Denmark A/S - 2009-05-12](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-denmark-as/3d69c2fc-294c-4631-960c-b370915da56d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 12, 2009

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