FDA Inspection
Teikoku Seiyaku Company, Ltd.Teikoku Seiyaku Company, Ltd. – FDA Inspection, Jul 6, 2018
Record Details
This FDA Inspection record concerns Teikoku Seiyaku Company, Ltd., with an inspection on July 6, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 3363cfd4-5d12-464a-b182-f7beb45c8f93
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1058444
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.165(a)Testing and release for distribution
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Other FDA inspections of Teikoku Seiyaku Company, Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 14, 2025 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 9, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 14, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 26, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Teikoku Seiyaku Company, Ltd.
- FDA Inspection 1258245 - 2025-02-14
- FDA Inspection 987969 - 2016-09-09
- FDA Inspection 873427 - 2014-03-14
- FDA Inspection 584346 - 2009-03-26
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