# Eurofins Biopharma Product Testing Sweden AB – FDA Inspection, Feb 16, 2011

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/aded8721-b5a2-45d0-b79a-336deb4ccda5
Source feed: FDA_Inspections

> FDA inspection 725045 of Eurofins Biopharma Product Testing Sweden AB, February 16, 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: 725045
- Company Name: Eurofins Biopharma Product Testing Sweden AB
- Inspection Date: 2011-02-16
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Pre-Approval Eval. of Animal Drugs and Food Additives
- Product Type: Veterinary
- Center: Animal Drugs & Feeds
- Office Name: Center for Veterinary Medicine
- Citation Count: 6

## Related Documents

- FDA Inspection 1273937 - 2024-06-19
- [FDA Inspection 1096830 - 2019-06-27](https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-sweden-ab/f5c45727-89ef-45e2-80c9-7e6e4e73df07)
- FDA Inspection 920664 - 2015-03-09

Company: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-sweden-ab/bf721e4e-7666-492d-9ab0-7b8ca39666eb

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