FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024
FDA inspection history on file, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483.
Cited most
Across all FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024 observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.192Production record review1
The complete FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024 file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-07-12 | 483 Form 483 | — | 2 | $99 |
Investigators on these documents
Carl Perez (1)Graeme Price (1)Jie He (1)Timothy Kamaldinov (1)
FEI number 3014382532 · most recent document Jul 12, 2024
About FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024
How many FDA Form 483s has FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024 received?
FDA Intel has 1 Form 483 on file for FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024; the most recent is dated Jul 12, 2024.
When was FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024 last inspected by FDA?
The most recent FDA inspection document on file for FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024 is a Form 483 dated Jul 12, 2024.
What did FDA cite at FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024?
The regulations cited most in the observations on file for FDA Form 483 Lonza Netherlands BV, Geleen, Netherlands, July 2024 are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.192 (Production record review), 1 time.