FDA Inspection 556188 — Janssen Pharmaceuticals Inc.

Janssen Pharmaceuticals Inc. — FEI 2211100

The FDA completed an inspection of Janssen Pharmaceuticals Inc. on Jan 15, 2009 in Raritan, NJ. 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
Jan 15, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Raritan, NJ (United States)