FDA Inspection 1101325 — Teva Pharmaceutical Industries

Teva Pharmaceutical Industries — FEI 3005202697

The FDA completed an inspection of Teva Pharmaceutical Industries on August 1, 2019 in Jerusalem. 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) (VAI)
End Date
August 1, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jerusalem (Israel)