FDA Inspection 653654 — Eurofins Biopharma Product Testing Australia Pty. Ltd.
The FDA completed an inspection of Eurofins Biopharma Product Testing Australia Pty. Ltd. on Mar 3, 2010 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
- Mar 3, 2010
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Girraween (Australia)