FDA Inspection
Tateyama Kasei Company Ltd.Tateyama Kasei Company Ltd. – FDA Inspection, Jul 5, 2017
Record Details
This FDA Inspection record concerns Tateyama Kasei Company Ltd., with an inspection on July 5, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 7483b02b-0657-44c6-8eb6-ae5a5cdbb1fc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1017463
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 11Electronic records
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Other FDA inspections of Tateyama Kasei Company Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 15, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Tateyama Kasei Company Ltd.
- FDA Inspection 1236028 - 2024-03-15
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