FDA Inspection 1011464 — 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 March 24, 2017 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
March 24, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Opava (Czech Republic)