FDA Inspection
L'OREAL USA, INC.L'OREAL USA, INC. – FDA Inspection, Dec 14, 2009
Record Details
This FDA Inspection record concerns L'OREAL USA, INC., with an inspection on December 14, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- L'OREAL USA, INC.
- Inspection Date
- December 14, 2009
- Product Type
- Drugs
View Company Profile
ID · b8d31189-3270-4e4d-a6a0-47a7391c9166
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 634549
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
8- 21 CFR 211.110(a)Control procedures to monitor and validate performance
- 21 CFR 211.160(a)Following/documenting laboratory controls
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.194(a)(7)Signatures and dates--person who performs test
- 21 CFR 211.84(d)(2)Reports of Analysis (Components)
- 21 CFR 211.22(c)Approve or reject procedures or specs
- 21 CFR 211.165(e)Test methods
- 21 CFR 211.198(a)Complaints reviewed by Quality Control Unit
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Other FDA inspections of L'OREAL USA, INC.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 24, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 12, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 30, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for L'OREAL USA, INC.
- FDA Inspection 1172731 - 2022-06-24
- FDA Inspection 989523 - 2016-08-12
- FDA Inspection 805325 - 2012-10-30
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