FDA Inspection 604140 — Synthon Argentina, SA
The FDA completed an inspection of Synthon Argentina, SA on Jul 10, 2009 in San Lorenzo. 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
- Jul 10, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- San Lorenzo (Argentina)