# Eurofins BioPharma Product Testing Columbia, LLC - Inspection Records

Source: https://www.globalkeysolutions.net/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. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1258161 - Eurofins BioPharma Product Testing Columbia, LLC - 2024-12-04](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/21aea860-5031-489d-b10a-3322fe5e07b1) — source: FDA, date: December 4, 2024
- [FDA Inspection 1161343 - Eurofins BioPharma Product Testing Columbia, LLC - 2022-01-14](https://www.globalkeysolutions.net/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](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/10651942-e5b2-4acf-be3f-dec43417e5dc) — classification: No Action Indicated (NAI), source: FDA, date: January 14, 2022
- [FDA Inspection 917473 - Eurofins BioPharma Product Testing Columbia, LLC - 2015-03-06](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/cafa03a7-c13d-4215-82a8-b908b640cd9c) — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2015
- [FDA Inspection 917473 - Eurofins BioPharma Product Testing Columbia, LLC - 2015-03-06](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/ee6211a0-e8ee-4c66-95eb-e10d282a7c15) — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2015
- [FDA Inspection 791170 - Eurofins BioPharma Product Testing Columbia, LLC - 2012-07-18](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/60b6f901-f807-4d17-b744-1bef795fa1ac) — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2012
- [FDA Inspection 762423 - Eurofins BioPharma Product Testing Columbia, LLC - 2011-12-16](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/7698890e-ed13-40e6-b44f-5ef674330562) — classification: No Action Indicated (NAI), source: FDA, date: December 16, 2011
- [FDA Inspection 658621 - Eurofins BioPharma Product Testing Columbia, LLC - 2010-04-23](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/3a1bba96-ee1b-4d8c-89ce-bcee4dd04eef) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2010
- [FDA Inspection 658621 - Eurofins BioPharma Product Testing Columbia, LLC - 2010-04-23](https://www.globalkeysolutions.net/records/fda_inspections/eurofins-biopharma-product-testing-columbia-llc/d969e0d1-c4cb-40a0-9dd5-2491212ade13) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2010

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