Lonza AG
FDA inspection history in Visp, Switzerland, 2017 to 2025
- 5
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2019: one Form 483; 2023: two Form 483s; 2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–19Two Form 483s, at Visp, Switzerland.
- 2019The longest 483 on file: 5 observations over 2 pages at Visp, Switzerland.
- 2023–25Three Form 483s, at Visp, Switzerland.
Cited most
Across all Lonza AG observations on file
- 21 CFR 211.100Written procedures; deviations2
- 21 CFR 211.110Sampling and testing of in-process materials and drug products2
- 21 CFR 211.194Laboratory records2
- 21 CFR 211.111Time limitations on production1
- 21 CFR 211.160General requirements1
The complete Lonza AG file.
All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
15% off buying them one by one
Sites
Visp, Switzerland
Five Form 483s · 2017 to 2025 · 12 observations
Latest: Form 483, Oct 28, 2025 →
Documents
5 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-10-28 | 483 Form 483 | Visp, Switzerland | 4 | $99 |
| 2023-03-28 | 483 Form 483 | Visp, Switzerland | 1 | $99 |
| 2023-03-28 | 483 Form 483 | Visp, Switzerland | 1 | $99 |
| 2019-03-29 | 483 Form 483 | Visp, Switzerland | 5 | $99 |
| 2017-12-15 | 483 Form 483 | Visp, Switzerland | 1 | $99 |
Investigators on these documents
Reyes Candau-Chacon (2)Ralph M. Bernstein (2)Lei Zhang (1)Maria Jose Lopez Barragan (1)Santos Comers (1)Tiara N. Brown-Crosen (1)Alexander Sohr (1)Vishal Patel (1)Frances Namuswe (1)
FEI number 3002930340 · most recent document Oct 28, 2025
About Lonza AG
How many FDA Form 483s has Lonza AG received?
FDA Intel has 5 Form 483s on file for Lonza AG; the most recent is dated Oct 28, 2025.
When was Lonza AG last inspected by FDA?
The most recent FDA inspection document on file for Lonza AG is a Form 483 dated Oct 28, 2025, for the site in Visp, Switzerland.
What did FDA cite at Lonza AG?
The regulations cited most in the observations on file for Lonza AG are 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 2 times; 21 CFR 211.194 (Laboratory records), 2 times.