FDA Inspection
Daiichi Sankyo Co., Ltd. Odawara PlantDaiichi Sankyo Co., Ltd. Odawara Plant – FDA Inspection, Jan 25, 2019
Record Details
This FDA Inspection record concerns Daiichi Sankyo Co., Ltd. Odawara Plant, with an inspection on January 25, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 59630dec-a3a1-4c89-a348-2502b37755dc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1081871
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Daiichi Sankyo Co., Ltd. Odawara Plant
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 15, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 20, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Daiichi Sankyo Co., Ltd. Odawara Plant
- FDA Inspection 971682 - 2016-04-15
- FDA Inspection 891670 - 2014-06-20
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