FDA Inspection
Shionogi Pharma Co., Ltd.Shionogi Pharma Co., Ltd. – FDA Inspection, Mar 15, 2019
Record Details
This FDA Inspection record concerns Shionogi Pharma Co., Ltd., with an inspection on March 15, 2019, issued by the Office of Inspections and Investigations, covering human drugs.
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ID · ca1f1877-b13e-44cf-a323-e47a17fbc49f
Inspection Facts
- Inspection number
- 1085190
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Shionogi Pharma Co., Ltd.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| July 1, 2025 | OAI | Office of Inspections and Investigations | Drug Quality Assurance |
| September 28, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 16, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 16, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 1, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shionogi Pharma Co., Ltd.
- FDA Inspection 1275087 - 2025-07-01
- FDA Inspection 1069417 - 2018-09-28
- FDA Inspection 1009607 - 2016-09-16
- FDA Inspection 1009606 - 2016-09-16
- FDA Inspection 874759 - 2014-04-01
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