FDA Inspection 578807 — Eurofins Biopharma Product Testing, Denmark A/S

Eurofins Biopharma Product Testing, Denmark A/S — FEI 3006272083

The FDA completed an inspection of Eurofins Biopharma Product Testing, Denmark A/S on May 12, 2009 in Glostrup. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.