FDA Inspection 1097960 — Teva Czech Industries s.r.o.

Teva Czech Industries s.r.o. — FEI 1000282452

The FDA completed an inspection of Teva Czech Industries s.r.o. on September 13, 2018 in Opava. 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
September 13, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Opava (Czech Republic)

Additional Details

Mutual Recognition Agreement (MRA)