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    Details of Akorn Inc's U.S. FDA Inspections. Original Data: FDA Inspection Database

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    Voluntary Action Indicated
    2009-06-01
    Decatur
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    62522-1038
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    2009-06-30
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    Voluntary Action Indicated
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    2009-11-10
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    Voluntary Action Indicated
    2010-09-17
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    Voluntary Action Indicated
    2010-09-17
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    2011-08-05
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    No Action Indicated
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    2012-05-25
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    2012-05-25
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    Voluntary Action Indicated
    2012-10-26
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    No Action Indicated
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    Voluntary Action Indicated
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    2009-06-12
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    Voluntary Action Indicated
    2011-05-19
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    2017-04-26
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    08512-3606
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