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 1022121.
Observations10
Issue DateMarch 31, 2017
StatusNo Warning Letter
Establishment TypeManufacturer
Related Inspections9
Establishment Details
Firm
Dixie Dew Products Inc
Location
Erlanger, Kentucky, United States
FEI Number
1022121
Establishment Type
Manufacturer
Product Type
Drugs
Issue Date
March 31, 2017
Country
United States
Inspection History, 2009 to 2017
NAI2
VAI3
OAI4
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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