FDA Inspection 1243943 — Eurofins Biolab S.R.L.
The FDA completed an inspection of Eurofins Biolab S.R.L. on Jun 25, 2024 in Vimodrone. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 25, 2024
- Fiscal Year
- 2024
- Product Type
- Veterinary
- Project Area
- Monitoring of Marketed Animal Drugs, Feed, and Devices
- Location
- Vimodrone (Italy)