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FDA Inspection 634116 — Janssen Cilag Manufacturing LLC

Janssen Cilag Manufacturing LLC — FEI 3006244497

The FDA completed an inspection of Janssen Cilag Manufacturing LLC on December 3, 2009 in Gurabo, PR. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 3, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Gurabo, PR (United States)

Facility

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