FDA Inspection 965139 — Janssen Pharmaceuticals Inc.

Janssen Pharmaceuticals Inc. — FEI 2211100

The FDA completed an inspection of Janssen Pharmaceuticals Inc. on Jan 22, 2016 in Raritan, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Raritan, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)