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FDA Inspection
•The Estee Lauder Inc.•February 23, 2010

The Estee Lauder Inc. – FDA Inspection, Feb 23, 2010

Record Details

This FDA Inspection record concerns The Estee Lauder Inc., with an inspection on February 23, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
The Estee Lauder Inc.
Inspection Date
February 23, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · c41ea593-3f64-4d65-9ca7-e5f884941a6f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
646115
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.115(a)Reprocessing procedures lack steps to be taken

Full citation text and observation details available on the Dashboard.

Other FDA inspections of The Estee Lauder Inc.

7
DateClassificationOfficeProject area
March 14, 2025Not classifiedNew York District Office
January 26, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 6, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 5, 2013VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
May 25, 2012VAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
View all 7 other inspections on the company page
Other documents for The Estee Lauder Inc.
  • FDA Inspection 1260025 - 2025-03-14
  • FDA Inspection 1038726 - 2018-01-26
  • FDA Inspection 938546 - 2015-08-06
  • FDA Inspection 843994 - 2013-08-05
  • FDA Inspection 783107 - 2012-05-25

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