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 3002930340.
Observations3
Issue DateOctober 28, 2025
StatusNo Warning Letter
Establishment TypeDrug Substance Manufacturer
Related Inspections8
Establishment Details
Firm
Lonza AG
Location
Visp, -, Switzerland
FEI Number
3002930340
Establishment Type
Drug Substance Manufacturer
Product Type
Drugs
Issue Date
October 28, 2025
Country
Switzerland
Inspection History, 2010 to 2023
NAI3
VAI5
NAI means No Action Indicated. VAI means Voluntary Action Indicated.
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