FDA Inspection 695835 — Teva Pharmaceutical Industries

Teva Pharmaceutical Industries — FEI 3005202697

The FDA completed an inspection of Teva Pharmaceutical Industries on September 16, 2010 in Jerusalem. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 16, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jerusalem (Israel)