# Eurofins BioPharma Product Testing Sweden AB, Uppsala, Sweden – FDA Inspections

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-sweden-ab/f001dd56-a1b0-463c-8b71-74a0939463de

> Inspection records and compliance data for Eurofins BioPharma Product Testing Sweden AB in Uppsala. 4 FDA inspections on record, last inspected December 08, 2022.

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## Details

- Name: Eurofins BioPharma Product Testing Sweden AB
- FEI Number: 3008763211
- Address Line 1: Rapsgatan 21
- City: Uppsala
- Country Name: Sweden
- Address: Rapsgatan 21, Uppsala, Sweden
- Country: Sweden

## Related Documents

- FDA Inspection 1233031 - Eurofins BioPharma Product Testing Sweden AB - 2022-12-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 8, 2022
- FDA Inspection 1016317 - Eurofins BioPharma Product Testing Sweden AB - 2017-05-12 — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2017
- FDA Inspection 1016317 - Eurofins BioPharma Product Testing Sweden AB - 2017-05-12 — classification: No Action Indicated (NAI), source: FDA, date: May 12, 2017
- [FDA Inspection 920666 - Eurofins BioPharma Product Testing Sweden AB - 2015-03-13](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/4390b5ec-da18-42c5-bfe0-424fa6dfb118) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 13, 2015
- FDA Inspection 725048 - Eurofins BioPharma Product Testing Sweden AB - 2011-02-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 18, 2011
- [FDA Inspection 725048 - Eurofins BioPharma Product Testing Sweden AB - 2011-02-18](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/3bc23b41-8917-4135-9efe-a98f59f54687) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 18, 2011

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