# Eurofins Lancaster Laboratories, Inc - Inspection Records

Source: https://www.keypedia.com/companies/eurofins-lancaster-laboratories-inc/a5676b12-3275-4a99-8f4b-3877e1728255

> Inspection records and compliance data for Eurofins Lancaster Laboratories, Inc in Portage, Michigan. Access full analysis and detailed observations.

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## Details

- Name: Eurofins Lancaster Laboratories, Inc
- FEI Number: 1833335
- City: Portage
- State: Michigan
- Country Name: United States
- Address Line 1: 6859 Quality Way
- Zip Code: 49002
- Business Operations: API/FDF ANALYTICAL TESTING

## Related Documents

- [483 - Eurofins Lancaster Laboratories, Inc - 2025-05-30](https://www.keypedia.com/records/483/eurofins-lancaster-laboratories-inc/4f724384-c3e2-4b72-bc92-271b07af7534) — source: FDA, date: May 30, 2025
- [FDA Inspection 1272016 - Eurofins Lancaster Laboratories, Inc - 2025-05-30](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/303e9119-e97b-46ac-953b-55ee592c5e2e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 30, 2025
- [FDA Inspection 1160560 - Eurofins Lancaster Laboratories, Inc - 2021-12-10](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/86599671-f9df-4681-8554-ac3c14a31631) — classification: No Action Indicated (NAI), source: FDA, date: December 10, 2021
- [FDA Inspection 1080439 - Eurofins Lancaster Laboratories, Inc - 2019-01-23](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/c157ed44-6c05-4072-8766-c1f056ecfae3) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2019
- [FDA Inspection 1045298 - Eurofins Lancaster Laboratories, Inc - 2018-02-23](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/6a2585c4-dfba-4218-be5e-6a17d5bc7184) — classification: No Action Indicated (NAI), source: FDA, date: February 23, 2018
- [FDA Inspection 1001348 - Eurofins Lancaster Laboratories, Inc - 2016-11-04](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/03b8ebaf-0c1b-4d04-9c72-145adf4c7ded) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2016
- [FDA Inspection 1001348 - Eurofins Lancaster Laboratories, Inc - 2016-11-04](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/19955c49-0273-4c87-b3d7-7aa5f1cbf109) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2016
- [FDA Inspection 889635 - Eurofins Lancaster Laboratories, Inc - 2014-08-01](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/efb068cd-3dde-4981-8fe6-60b3c544ac7c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 1, 2014
- [FDA Inspection 889635 - Eurofins Lancaster Laboratories, Inc - 2014-08-01](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/9af92fde-b6b9-4887-be63-ce02c3ecb9cc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 1, 2014
- [FDA Inspection 889635 - Eurofins Lancaster Laboratories, Inc - 2014-08-01](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/190102da-bf3d-4692-92df-2e23019cd654) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 1, 2014
- [FDA Inspection 778568 - Eurofins Lancaster Laboratories, Inc - 2012-04-25](https://www.keypedia.com/records/fda_inspections/eurofins-lancaster-laboratories-inc/c7749cb3-c5a6-4b6e-bd4b-0de95dc988e6) — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2012

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