Source: FDA, document on file. FDA released the Form 483 itself. The document linked above is our copy of FDA's file, stored by us so the link cannot break, and FDA's own copy is linked beside it. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3003102962.
Observations2
Issue DateJuly 11, 2015
Status2 Related Warning Letters
Establishment TypeDrug Manufacturer
Related Inspections5
Establishment Details
Firm
Akorn, Inc.
Location
Gurnee, Illinois, United States
FEI Number
3003102962
Establishment Type
Drug Manufacturer
Product Type
Drugs
Issue Date
July 11, 2015
Country
United States
Inspection History, 2009 to 2019
NAI4
VAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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