FDA Inspection
Ishihara Sangyo Kaisha, Ltd.Ishihara Sangyo Kaisha, Ltd. – FDA Inspection, Sep 8, 2017
Record Details
This FDA Inspection record concerns Ishihara Sangyo Kaisha, Ltd., with an inspection on September 8, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 92560ad6-febf-447e-8d8a-e7dc9a35caf0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1028577
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Ishihara Sangyo Kaisha, Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 9, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 5, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 2, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Ishihara Sangyo Kaisha, Ltd.
- FDA Inspection 1181874 - 2022-09-09
- FDA Inspection 895933 - 2014-09-05
- FDA Inspection 747053 - 2011-09-02
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