FDA Inspection 592212 — Eurofins Biolab S.R.L.
The FDA completed an inspection of Eurofins Biolab S.R.L. on May 20, 2009 in Vimodrone. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 20, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Vimodrone (Italy)