Estee Lauder N.V.
FDA inspection history in Oevel, Belgium, 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, at Oevel, Belgium.
Cited most
Across all Estee Lauder N.V. observations on file
- 21 CFR 211.84(d)(2)Testing and approval or rejection of components, drug product containers, and closures1
The complete Estee Lauder N.V. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Oevel, Belgium
One Form 483 · 2024 · 1 observation
Latest: Form 483, Apr 26, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-04-26 | 483 Form 483 | Oevel, Belgium | 1 | $99 |
Investigators on these documents
FEI number 1000224360 · most recent document Apr 26, 2024
About Estee Lauder N.V.
How many FDA Form 483s has Estee Lauder N.V. received?
FDA Intel has 1 Form 483 on file for Estee Lauder N.V.; the most recent is dated Apr 26, 2024.
When was Estee Lauder N.V. last inspected by FDA?
The most recent FDA inspection document on file for Estee Lauder N.V. is a Form 483 dated Apr 26, 2024, for the site in Oevel, Belgium.
What did FDA cite at Estee Lauder N.V.?
The regulations cited most in the observations on file for Estee Lauder N.V. are 21 CFR 211.84(d)(2) (Testing and approval or rejection of components, drug product containers, and closures), 1 time.