Janssen Ortho Llc | FDA | Inspections | Form 483 | Warning Letters | PharmaCompass.com
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    Details of Janssen Ortho Llc's U.S. FDA Inspections. Original Data: FDA Inspection Database

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    No Action Indicated
    2012-06-19
    Raritan
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    2012-06-28
    Titusville
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    08560-1503
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    No Action Indicated
    2009-03-27
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    30601-1645
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    No Action Indicated
    2011-02-18
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    Voluntary Action Indicated
    2009-01-15
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    No Action Indicated
    2009-04-09
    Titusville
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    08560-1503
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    No Action Indicated
    2010-08-06
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    08869-1425
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    Voluntary Action Indicated
    2010-12-09
    Titusville
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    08560-1503
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    No Action Indicated
    2011-06-01
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    08560-1503
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    No Action Indicated
    2011-08-22
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