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FDA Inspection
•L'Oreal Usa, Inc.•September 30, 2022

L'Oreal Usa, Inc. – FDA Inspection, Sep 30, 2022

Record Details

This FDA Inspection record concerns L'Oreal Usa, Inc., with an inspection on September 30, 2022, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
L'Oreal Usa, Inc.
Inspection Date
September 30, 2022
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ff4eaf07-ef0d-4604-8fde-a2d976c81720

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1181302
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

4
  1. 21 CFR 211.100(a)Changes to Procedures Not Reviewed, Approved
  2. 21 CFR 211.160(a)Deviations from laboratory control requirements
  3. 21 CFR 211.113(a)Procedures for non-sterile drug products
  4. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of L'Oreal Usa, Inc.

6
DateClassificationOfficeProject area
September 18, 2026Not classifiedCincinnati District Office
April 1, 2026Not classifiedCincinnati District OfficeDrug Quality Assurance
September 27, 2024NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
February 11, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 18, 2011NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
View all 6 other inspections on the company page
Other documents for L'Oreal Usa, Inc.
  • FDA Inspection 1291960 - 2026-09-18
  • FDA Inspection 1302452 - 2026-04-01
  • FDA Inspection 1235605 - 2024-09-27
  • FDA Inspection 961108 - 2016-02-11
  • FDA Inspection 724058 - 2011-04-18

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