FDA Inspection 1210122 — Janssen Pharmaceutica N.V.

Janssen Pharmaceutica N.V. — FEI 3002807337

The FDA completed an inspection of Janssen Pharmaceutica N.V. on Oct 27, 2022 in Geel. 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
Oct 27, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Geel (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)