FDA Inspection 1338366 — 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 Aug 30, 2024 in Opava. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 30, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Opava (Czech Republic)

Additional Details

Mutual Recognition Agreement (MRA)