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

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    01 AmbioPharm, Inc (5)

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    01 2017-07-05 (1)

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    No Action Indicated
    2011-08-16
    Beech Island
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    29842-9404
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    Voluntary Action Indicated
    2013-03-28
    Beech Island
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    29842-9404
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    Voluntary Action Indicated
    2014-10-09
    Beech Island
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    29842-9404
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    Voluntary Action Indicated
    2017-07-05
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    29842-9404
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    No Action Indicated
    2016-01-29
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    Voluntary Action Indicated
    2013-08-30
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    No Action Indicated
    2008-11-04
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