FDA Inspection
Daito Kasei Kogyo Co., Ltd.Daito Kasei Kogyo Co., Ltd. – FDA Inspection, Jul 21, 2017
Record Details
This FDA Inspection record concerns Daito Kasei Kogyo Co., Ltd., with an inspection on July 21, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 8c9a010c-9eee-4549-8889-0f555dda1ab8
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 1020787
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
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