# Eurofins BioPharma Product Testing Czech Republic s.r.o., Brno-Jih, Czech Republic – FDA Inspections

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-czech-republic-sro/2d5e4f85-9d30-4abf-b019-3129dbffe3ca

> Inspection records and compliance data for Eurofins BioPharma Product Testing Czech Republic s.r.o. in Brno-Jih. 5 FDA inspections on record, last inspected July 24, 2024.

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## Details

- Name: Eurofins BioPharma Product Testing Czech Republic s.r.o.
- FEI Number: 3008920466
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: Videnska 204/125
- City: Brno-Jih
- Country Name: Czech Republic
- Address: Videnska 204/125, Brno-Jih, Czech Republic
- Country: Czech Republic

## Related Documents

- FDA Inspection 1270980 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - 2024-07-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 24, 2024
- FDA Inspection 1134811 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - 2020-07-16 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 16, 2020
- [FDA Inspection 988104 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - 2016-08-09](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-czech-republic-sro/c3e2c10c-50e5-4a31-be1d-0954bd2f1035) — classification: No Action Indicated (NAI), source: FDA, date: August 9, 2016
- FDA Inspection 892490 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - 2014-07-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 29, 2014
- [FDA Inspection 892490 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - 2014-07-29](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-czech-republic-sro/cca7e136-ec3b-4624-bca0-a5e63ae6a4d7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 29, 2014
- FDA Inspection 727383 - Eurofins BioPharma Product Testing Czech Republic s.r.o. - 2011-05-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 20, 2011

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