FDA Inspection 819622 — Janssen Ortho LLC

Janssen Ortho LLC — FEI 3002942061

The FDA completed an inspection of Janssen Ortho LLC on February 22, 2013 in Gurabo, PR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 22, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gurabo, PR (United States)