Lonza AG — FDA Facility Profile
Lonza AG is an FDA-registered facility (FEI 3002930340) located in Visp, CH. Registered operations: ANALYSIS; API MANUFACTURE. RegDataLab tracks 8 FDA inspections at this facility.
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What FDA found at this site
- Latest inspection
- Mar 28, 2023: Voluntary Action Indicated (VAI)
- Inspections on record
- 8 (5 VAI, 3 NAI)
- Last OAI inspection
- None on record
- Warning letters
- None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
- Form 483 and inspection documents
- 2 in FDA's reading room
- Import refusals
- 5
Inspections and what FDA cited
| Date | Result | What FDA cited |
|---|---|---|
| Mar 28, 2023 | Voluntary Action Indicated (VAI) | No citations listed |
| Dec 15, 2017 | Voluntary Action Indicated (VAI) | No citations listed |
| Mar 11, 2016 | Voluntary Action Indicated (VAI) | No citations listed |
| Aug 29, 2014 | Voluntary Action Indicated (VAI) | No citations listed |
| Apr 2, 2014 | No Action Indicated (NAI) | No citations listed |
| Apr 12, 2013 | No Action Indicated (NAI) | No citations listed |
| Sep 18, 2012 | No Action Indicated (NAI) | No citations listed |
| Jun 24, 2010 | Voluntary Action Indicated (VAI) | No citations listed |
Form 483s and inspection documents
- Oct 28, 2025: 483 on FDA.gov
- Mar 28, 2023: 483 on FDA.gov
Facility details
- Company
- Lonza AG
- Location
- Visp (CH)
- Registration Expires
- Dec 31, 2026
- Operations
- ANALYSIS; API MANUFACTURE
- Source
- decrs