FDA Inspection
Nippon Kayaku Co., Ltd.Nippon Kayaku Co., Ltd. – FDA Inspection, Jul 10, 2018
Record Details
This FDA Inspection record concerns Nippon Kayaku Co., Ltd., with an inspection on July 10, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 2ef895a3-94c1-4440-9161-179bdd90fa15
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1059447
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Nippon Kayaku Co., Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| December 3, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 27, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 24, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Nippon Kayaku Co., Ltd.
- FDA Inspection 951969 - 2015-12-03
- FDA Inspection 802599 - 2012-09-27
- FDA Inspection 783742 - 2012-05-24
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