FDA Inspection 1341150 — Novo Nordisk A/S - KV

Novo Nordisk A/S - KV — FEI 3015545250

The FDA completed an inspection of Novo Nordisk A/S - KV on May 2, 2024 in Varlose. 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
May 2, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Varlose (Denmark)

Additional Details

Mutual Recognition Agreement (MRA)