FDA Inspection
Shiseido America Inc.Shiseido America Inc. – FDA Inspection, Dec 3, 2024
Record Details
This FDA Inspection record concerns Shiseido America Inc., with an inspection on December 3, 2024, issued by the New Jersey District Office, covering human drugs.
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ID · 68067437-a547-4342-be3b-9d8fd684010b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1254656
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.142(b)Storage under appropriate conditions
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
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Other FDA inspections of Shiseido America Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 1, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 26, 2017 | VAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| May 13, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 12, 2012 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| November 24, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shiseido America Inc.
- FDA Inspection 1070566 - 2018-11-01
- FDA Inspection 1002794 - 2017-01-26
- FDA Inspection 877354 - 2014-05-13
- FDA Inspection 776775 - 2012-04-12
- FDA Inspection 633380 - 2009-11-24
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