FDA Inspection 1296030 — Janssen Pharmaceutica, N.V.

Janssen Pharmaceutica, N.V. — FEI 3002807336

The FDA completed an inspection of Janssen Pharmaceutica, N.V. on May 12, 2025 in Beerse. 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 12, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Beerse (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)

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