# Eurofins Biopharma Product Testing Sweden AB - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-sweden-ab/bf721e4e-7666-492d-9ab0-7b8ca39666eb

> Inspection records and compliance data for Eurofins Biopharma Product Testing Sweden AB in Uppsala, None. Access full analysis and detailed observations.

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## Details

- Name: Eurofins Biopharma Product Testing Sweden AB
- FEI Number: 3008759559
- City: Uppsala
- State: None
- Country Name: Sweden
- Address Line 1: Virdings Alle 2
- Zip Code: None

## Related Documents

- [FDA Inspection 1273937 - Eurofins Biopharma Product Testing Sweden AB - 2024-06-19](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/f63aee81-a88e-4c26-ad78-f8abdd8cb8f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 19, 2024
- [FDA Inspection 1096830 - Eurofins Biopharma Product Testing Sweden AB - 2019-06-27](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/cb2ce598-37c2-420e-8511-3afd4c2c296d) — classification: No Action Indicated (NAI), source: FDA, date: June 27, 2019
- [FDA Inspection 1096830 - Eurofins Biopharma Product Testing Sweden AB - 2019-06-27](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/f5c45727-89ef-45e2-80c9-7e6e4e73df07) — classification: No Action Indicated (NAI), source: FDA, date: June 27, 2019
- [FDA Inspection 920664 - Eurofins Biopharma Product Testing Sweden AB - 2015-03-09](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/29a2e242-d3a6-40e2-a2f9-3008c389bc8e) — classification: No Action Indicated (NAI), source: FDA, date: March 9, 2015
- [FDA Inspection 725045 - Eurofins Biopharma Product Testing Sweden AB - 2011-02-16](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/8ae8d705-181e-40dc-a8da-ca998aea5d6d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 16, 2011
- [FDA Inspection 725045 - Eurofins Biopharma Product Testing Sweden AB - 2011-02-16](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/aded8721-b5a2-45d0-b79a-336deb4ccda5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 16, 2011

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