FDA Inspection 1180012 — Eurofarma Laboratorios S.A.
The FDA completed an inspection of Eurofarma Laboratorios S.A. on Sep 20, 2022 in Itapevi. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 20, 2022
- Fiscal Year
- 2022
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Itapevi (Brazil)