FDA Inspection 1292060 — Novo Nordisk US Bio Production Inc.

Novo Nordisk US Bio Production Inc. — FEI 3012593913

The FDA completed an inspection of Novo Nordisk US Bio Production Inc. on December 9, 2025 in West Lebanon, NH. 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
December 9, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Lebanon, NH (United States)