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 3008927138.
Observations3
Issue DateAugust 31, 2018
StatusNo Warning Letter
Establishment TypeProducer of Sterile Drug Products
Related Inspections2
Establishment Details
Firm
Morton Drug Company dba Morton LTC
Location
Neenah, Wisconsin, United States
FEI Number
3008927138
Establishment Type
Producer of Sterile Drug Products
Product Type
Drugs
Issue Date
August 31, 2018
Country
United States
Inspection History, 2011 to 2015
VAI1
OAI1
VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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