# Eurofins Biopharma Product Testing, Denmark A/S – FDA Inspection, Jun 22, 2016

Source: https://www.keypedia.com/records/fda_inspections/eurofins-biopharma-product-testing-denmark-as/aef8fe15-3be8-45e4-b1ad-0b861b1efd96
Source feed: FDA_Inspections

> FDA inspection 976102 of Eurofins Biopharma Product Testing, Denmark A/S, June 22, 2016. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 211. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 976102
- Company Name: Eurofins Biopharma Product Testing, Denmark A/S
- Inspection Date: 2016-06-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 5

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Company: https://www.keypedia.com/companies/eurofins-biopharma-product-testing-denmark-as/b229d16c-8c5e-4288-9c41-ff6ea8ba3df5

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