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 3002807108.
Observations2
Issue DateMay 22, 2023
StatusNo Warning Letter
Establishment TypeDrug Manufacturer
Related Inspections9
Establishment Details
Firm
Sanofi S.r.l.
Location
Anagni, -, Italy
FEI Number
3002807108
Establishment Type
Drug Manufacturer
Product Type
Drugs
Issue Date
May 22, 2023
Country
Italy
Inspection History, 2011 to 2024
NAI1
VAI8
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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