# Eurofins BioPharma Product Testing Columbia, LLC, Columbia, MO – FDA Inspections

Source: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-columbia-llc/b616a9a6-094c-4f02-80ba-59880916eaf2

> Inspection records and compliance data for Eurofins BioPharma Product Testing Columbia, LLC in Columbia, Missouri. 8 FDA inspections on record, last inspected December 04, 2024.

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## Details

- Name: Eurofins BioPharma Product Testing Columbia, LLC
- FEI Number: 3007069176
- Business Operations: API/FDF ANALYTICAL TESTING
- Address Line 1: 4780 Discovery Dr
- City: Columbia
- State: Missouri
- Zip Code: 65201
- Country Name: United States
- Address: 4780 Discovery Dr, Columbia, Missouri 65201, United States
- Country: United States

## Related Documents

- FDA Inspection 1258161 - Eurofins BioPharma Product Testing Columbia, LLC - 2024-12-04 — source: FDA, date: December 4, 2024
- [FDA Inspection 1161343 - Eurofins BioPharma Product Testing Columbia, LLC - 2022-01-14](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/eba63794-537e-48f1-a247-1601e534152e) — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2022
- FDA Inspection 1161343 - Eurofins BioPharma Product Testing Columbia, LLC - 2022-01-14 — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2022
- FDA Inspection 1065874 - Eurofins BioPharma Product Testing Columbia, LLC - 2018-08-15 — source: FDA, date: August 15, 2018
- FDA Inspection 999122 - Eurofins BioPharma Product Testing Columbia, LLC - 2017-01-26 — source: FDA, date: January 26, 2017
- FDA Inspection 917473 - Eurofins BioPharma Product Testing Columbia, LLC - 2015-03-06 — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2015
- FDA Inspection 917473 - Eurofins BioPharma Product Testing Columbia, LLC - 2015-03-06 — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2015
- FDA Inspection 791170 - Eurofins BioPharma Product Testing Columbia, LLC - 2012-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2012
- FDA Inspection 762423 - Eurofins BioPharma Product Testing Columbia, LLC - 2011-12-16 — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2011
- FDA Inspection 658621 - Eurofins BioPharma Product Testing Columbia, LLC - 2010-04-23 — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2010

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