# Eurofins PROXY Laboratories B.V. - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-proxy-laboratories-bv/f285c14e-3524-4cb3-8bd8-767736fdfa78

> Inspection records and compliance data for Eurofins PROXY Laboratories B.V. in Leiden, None. Access full analysis and detailed observations.

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## Details

- Name: Eurofins PROXY Laboratories B.V.
- FEI Number: 3004939239
- City: Leiden
- State: None
- Country Name: Netherlands
- Address Line 1: Archimedesweg 25
- Zip Code: None
- Business Operations: API/FDF ANALYTICAL TESTING, FDF MANUFACTURE, PACK

## Related Documents

- [483 - Eurofins PROXY Laboratories B.V. - 2023-11-10](https://www.keypedia.com/records/483/eurofins-proxy-laboratories-bv/bfb8e0de-09f4-4e03-83ff-5f9f164ae505) — source: FDA, date: November 10, 2023
- [FDA Inspection 1223518 - Eurofins PROXY Laboratories B.V. - 2023-11-10](https://www.keypedia.com/records/fda_inspections/eurofins-proxy-laboratories-bv/0fdf7346-daaf-4922-91a1-672687346725) — source: FDA, date: November 10, 2023
- [FDA Inspection 1272071 - Eurofins PROXY Laboratories B.V. - 2022-07-01](https://www.keypedia.com/records/fda_inspections/eurofins-proxy-laboratories-bv/39208e98-d17b-4de0-8630-d7c48e4ddbf6) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 1, 2022
- [FDA Inspection 1142875 - Eurofins PROXY Laboratories B.V. - 2019-05-01](https://www.keypedia.com/records/fda_inspections/eurofins-proxy-laboratories-bv/a474b808-9fd7-43bd-948d-d948cff0e2b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2019
- [FDA Inspection 987725 - Eurofins PROXY Laboratories B.V. - 2016-09-16](https://www.keypedia.com/records/fda_inspections/eurofins-proxy-laboratories-bv/6ae8901a-a9cb-4950-95de-9854785ee308) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 16, 2016
- [FDA Inspection 823838 - Eurofins PROXY Laboratories B.V. - 2013-03-18](https://www.keypedia.com/records/fda_inspections/eurofins-proxy-laboratories-bv/75819ee2-ab1b-4506-b843-353da3d5f9b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 18, 2013

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