FDA Inspection 1100788 — Protalix Ltd.
The FDA completed an inspection of Protalix Ltd. on Jul 11, 2019 in Karmi'El. 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 11, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Karmi'El (Israel)