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 3004762406.
Observations11
Issue DateJune 27, 2025
StatusNo Warning Letter
Establishment TypeDrug Manufacturer
Related Inspections7
Establishment Details
Firm
NerPharMa S.r.l.
Location
Nerviano, -, Italy
FEI Number
3004762406
Establishment Type
Drug Manufacturer
Product Type
Drugs
Issue Date
June 27, 2025
Country
Italy
Inspection History, 2009 to 2024
NAI2
VAI5
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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