FDA Inspection
Sumitomo Chemical Co., Ltd.Sumitomo Chemical Co., Ltd. – FDA Inspection, Sep 6, 2019
Record Details
This FDA Inspection record concerns Sumitomo Chemical Co., Ltd., with an inspection on September 6, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · ad631885-7432-4f4d-b3ee-fda2d9247f93
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1101409
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Sumitomo Chemical Co., Ltd.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2025 | Not classified | Office of Inspections and Investigations | |
| December 8, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 23, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 14, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 18, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sumitomo Chemical Co., Ltd.
- FDA Inspection 1293378 - 2025-10-31
- FDA Inspection 1037183 - 2017-12-08
- FDA Inspection 988028 - 2016-09-23
- FDA Inspection 875356 - 2014-03-14
- FDA Inspection 673967 - 2010-06-18
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