FDA Inspection 1311564 — TEVA Pharmaceuticals USA, Inc.

TEVA Pharmaceuticals USA, Inc. — FEI 2245641

The FDA completed an inspection of TEVA Pharmaceuticals USA, Inc. on Jul 20, 2026 in Fairfield, NJ. 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 20, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fairfield, NJ (United States)

Citations

IDCFRDescription
359221 CFR 211.110(c)In-process materials characteristics testing

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