# FDA Inspection 1268950 - Eurofins BioPharma Product Testing Switzerland AG - January 23, 2025

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-switzerland-ag/0c42e8ce-4eac-42c3-885d-f4595e2ce269
Source feed: FDA_Inspections

> FDA Inspection 1268950 for Eurofins BioPharma Product Testing Switzerland AG on January 23, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1268950
- Company Name: Eurofins BioPharma Product Testing Switzerland AG
- Inspection Date: 2025-01-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

Company: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-switzerland-ag/106629c3-3d43-4c58-b07c-eeba64b823ce

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c