# FDA Inspection 920666 - Eurofins BioPharma Product Testing Sweden AB - March 13, 2015

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/4390b5ec-da18-42c5-bfe0-424fa6dfb118
Source feed: FDA_Inspections

> FDA Inspection 920666 for Eurofins BioPharma Product Testing Sweden AB on March 13, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 920666
- Company Name: Eurofins BioPharma Product Testing Sweden AB
- Inspection Date: 2015-03-13
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Monitoring of Marketed Animal Drugs, Feed, and Devices
- Product Type: Veterinary
- Office Name: Center for Veterinary Medicine

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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