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 3000210731.
Observations8
Issue DateJuly 11, 2015
StatusNo Warning Letter
Establishment TypeDrug Manufacturer
Related Inspections6
Establishment Details
Firm
Eon Labs Inc
Issued To
Sandoz, Inc.
Location
Wilson, North Carolina, United States
FEI Number
3000210731
Establishment Type
Drug Manufacturer
Product Type
Drugs
Issue Date
July 11, 2015
Country
United States
Inspection History, 2009 to 2019
NAI3
VAI2
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.
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