# Eurofins BioPharma Product Testing Spain SLU - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-spain-slu/06d9c739-dbbe-492a-9941-74f432014092

> Inspection records and compliance data for Eurofins BioPharma Product Testing Spain SLU in Esplugues De Llobregat, None. Access full analysis and detailed observations.

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## Details

- Name: Eurofins BioPharma Product Testing Spain SLU
- FEI Number: 3007914833
- City: Esplugues De Llobregat
- State: None
- Country Name: Spain
- Address Line 1: Calle De Josep Argemi 13-15
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [FDA Inspection 1279238 - Eurofins BioPharma Product Testing Spain SLU - 2025-06-19](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-spain-slu/cc66e41e-84ca-4a3c-91c6-85dd7c8d41c9) — source: FDA, date: June 19, 2025
- [FDA Inspection 1279238 - Eurofins BioPharma Product Testing Spain SLU - 2025-06-19](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-spain-slu/52c02bdd-96f0-4295-8553-f8d85d337abf) — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2025
- [FDA Inspection 1285158 - Eurofins BioPharma Product Testing Spain SLU - 2022-01-13](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-spain-slu/75c67a9d-d4a7-4850-bdfa-496213a7263b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2022
- [FDA Inspection 1134791 - Eurofins BioPharma Product Testing Spain SLU - 2018-11-06](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-spain-slu/2449d1dd-d952-445b-9749-0e72188f38a5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 6, 2018
- [FDA Inspection 986616 - Eurofins BioPharma Product Testing Spain SLU - 2016-06-29](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-spain-slu/b9c0be53-1de7-4efc-98e1-5ddc982c9d7e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 29, 2016

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