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FDA Inspection 638139 — Janssen Cilag Manufacturing LLC

Janssen Cilag Manufacturing LLC — FEI 3006244497

The FDA completed an inspection of Janssen Cilag Manufacturing LLC on December 16, 2009 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
December 16, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gurabo, PR (United States)

Facility

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FDA data resources