FDA Inspection 813048 — Synthon Argentina, SA
The FDA completed an inspection of Synthon Argentina, SA on Dec 7, 2012 in San Lorenzo. 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
- Dec 7, 2012
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- San Lorenzo (Argentina)