# Eurofins BioPharma Product Testing Sweden AB – FDA Inspection, Feb 18, 2011

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/3bc23b41-8917-4135-9efe-a98f59f54687
Source feed: FDA_Inspections

> FDA inspection 725048 of Eurofins BioPharma Product Testing Sweden AB, February 18, 2011. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 211. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 725048
- Company Name: Eurofins BioPharma Product Testing Sweden AB
- Inspection Date: 2011-02-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Monitoring of Marketed Animal Drugs, Feed, and Devices
- Product Type: Veterinary
- Center: Animal Drugs & Feeds
- Office Name: Center for Veterinary Medicine
- Citation Count: 6

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- [FDA Inspection 920666 - 2015-03-13](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/4390b5ec-da18-42c5-bfe0-424fa6dfb118)

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