# FDA Inspection 1016317 - Eurofins BioPharma Product Testing Sweden AB - May 12, 2017

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/a0b7aa65-d9fc-4a1b-83fa-62bb40351ae4
Source feed: FDA_Inspections

> FDA Inspection 1016317 for Eurofins BioPharma Product Testing Sweden AB on May 12, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1016317
- Company Name: Eurofins BioPharma Product Testing Sweden AB
- Inspection Date: 2017-05-12
- Classification: No Action Indicated (NAI)
- Project Area: Monitoring of Marketed Animal Drugs, Feed, and Devices
- Product Type: Veterinary
- Office Name: Center for Veterinary Medicine

## Related Documents

- [FDA Inspection 1233031 - 2022-12-08](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/315dda0b-e7ae-4483-8126-84366c86c4f6)
- [FDA Inspection 1016317 - 2017-05-12](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/e7e0eb94-0e14-4e3b-819a-a2277058bcbc)
- [FDA Inspection 920666 - 2015-03-13](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/4390b5ec-da18-42c5-bfe0-424fa6dfb118)
- [FDA Inspection 725048 - 2011-02-18](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/1634d0db-90fb-41af-9420-b8e1f99db8d4)
- [FDA Inspection 725048 - 2011-02-18](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/3bc23b41-8917-4135-9efe-a98f59f54687)

Company: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-sweden-ab/f001dd56-a1b0-463c-8b71-74a0939463de

Office: https://www.keypedia.com/offices/center-for-veterinary-medicine/7e30a309-56e4-4e7a-8b8b-e07674bb07b4