FDA Inspection
The Estee Lauder Inc.The Estee Lauder Inc. – FDA Inspection, May 25, 2011
Record Details
This FDA Inspection record concerns The Estee Lauder Inc., with an inspection on May 25, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- The Estee Lauder Inc.
- Inspection Date
- May 25, 2011
- Product Type
- Drugs
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ID · 462c1fa2-79a2-4b5a-b82b-796571c72b63
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 725633
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
6- 21 CFR 211.166(b)Adequate number of batches on stability
- 21 CFR 211.188(b)(11)Identification of persons involved, each significant step
- 21 CFR 211.188(b)(2)Identity of major equipment and lines used
- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
- 21 CFR 211.165(a)Testing and release for distribution
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Other FDA inspections of The Estee Lauder Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| March 14, 2025 | Not classified | New York District Office | |
| January 26, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 6, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 5, 2013 | VAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| May 25, 2012 | VAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
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