# Eurofins Biolab S.r.l., Vimodrone, Italy – FDA Inspections

Source: https://www.keypedia.com/companies/eurofins-biolab-srl/3f1b31b8-2af2-4083-8cdb-3e0fbf994b22

> Inspection records and compliance data for Eurofins Biolab S.r.l. in Vimodrone. 6 FDA inspections on record, 1 Form 483, last inspected September 13, 2024.

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## Details

- Name: Eurofins Biolab S.r.l.
- FEI Number: 3002806530
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: Via Bruno Buozzi 2
- City: Vimodrone
- Country Name: Italy
- Address: Via Bruno Buozzi 2, Vimodrone, Italy
- Country: Italy

## Related Documents

- FDA Inspection 1261441 - Eurofins Biolab S.r.l. - 2024-09-13 — source: FDA, date: September 13, 2024
- FDA Inspection 1261441 - Eurofins Biolab S.r.l. - 2024-09-13 — source: FDA, date: September 13, 2024
- FDA Inspection 1261441 - Eurofins Biolab S.r.l. - 2024-09-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2024
- FDA Inspection 1261441 - Eurofins Biolab S.r.l. - 2024-09-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2024
- [FDA Inspection 1243943 - Eurofins Biolab S.r.l. - 2024-06-25](https://www.keypedia.com/records/fda_inspections/eurofins-biolab-srl/81f398ba-ef59-4d55-a222-76e0e91251e6) — classification: No Action Indicated (NAI), source: FDA, date: June 25, 2024
- FDA Inspection 1123754 - Eurofins Biolab S.r.l. - 2018-10-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 5, 2018
- [FDA Inspection 1049127 - Eurofins Biolab S.r.l. - 2018-04-18](https://www.keypedia.com/records/fda_inspections/eurofins-biolab-srl/a3d20d2a-7039-44c7-af6c-05bb31d98ac1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2018
- FDA Inspection 1049127 - Eurofins Biolab S.r.l. - 2018-04-18 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 18, 2018
- FDA Inspection 929781 - Eurofins Biolab S.r.l. - 2015-05-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 21, 2015
- FDA Inspection 592212 - Eurofins Biolab S.r.l. - 2009-05-20 — classification: No Action Indicated (NAI), source: FDA, date: May 20, 2009

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