L'Oreal USA, Inc.
FDA inspection history in FLORENCE, Kentucky, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at FLORENCE, Kentucky.
Cited most
Across all L'Oreal USA observations on file
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete L'Oreal USA file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
FLORENCE, Kentucky
One Form 483 · 2022 · 4 observations
Latest: Form 483, Sep 30, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-09-30 | 483 Form 483 | FLORENCE, Kentucky | 4 | $99 |
Investigators on these documents
FEI number 3003763470 · most recent document Sep 30, 2022
About L'Oreal USA, Inc.
How many FDA Form 483s has L'Oreal USA, Inc. received?
FDA Intel has 1 Form 483 on file for L'Oreal USA, Inc.; the most recent is dated Sep 30, 2022.
When was L'Oreal USA, Inc. last inspected by FDA?
The most recent FDA inspection document on file for L'Oreal USA, Inc. is a Form 483 dated Sep 30, 2022, for the site in FLORENCE, Kentucky.
What did FDA cite at L'Oreal USA, Inc.?
The regulations cited most in the observations on file for L'Oreal USA, Inc. are 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.160(a) (General requirements), 1 time.