FDA Inspection
Shiseido Co., LTDShiseido Co., LTD – FDA Inspection, Aug 1, 2014
Record Details
This FDA Inspection record concerns Shiseido Co., LTD, with an inspection on August 1, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Shiseido Co., LTD
- Inspection Date
- August 1, 2014
- Product Type
- Drugs
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ID · f8acb322-30f0-467b-8fc7-0094bd92dfa9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 895043
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.160(b)(1)Incoming lots - conformance to written specs-
- 21 CFR 211.165(e)Test methods
- 21 CFR 211.67(b)Written procedures fail to include
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Other FDA inspections of Shiseido Co., LTD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 27, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 12, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shiseido Co., LTD
- FDA Inspection 1075263 - 2018-11-27
- FDA Inspection 781294 - 2012-04-12
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