FDA Inspection 845397 — Eurofins Biopharma Product Testing Australia Pty. Ltd.
The FDA completed an inspection of Eurofins Biopharma Product Testing Australia Pty. Ltd. on Jul 24, 2013 in Girraween. 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.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 24, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Girraween (Australia)