FDA Inspection
Shionogi Pharma Co., Ltd.Shionogi Pharma Co., Ltd. – FDA Inspection, Jul 26, 2010
Record Details
This FDA Inspection record concerns Shionogi Pharma Co., Ltd., with an inspection on July 26, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Shionogi Pharma Co., Ltd.
- Inspection Date
- July 26, 2010
- Product Type
- Drugs
View Company Profile
ID · 47f247bf-c348-455d-b494-1c30f4afd410
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 676812
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
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 |
| March 15, 2019 | Not classified | Office of Inspections and Investigations | |
| 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 |
Other documents for Shionogi Pharma Co., Ltd.
- FDA Inspection 1275087 - 2025-07-01
- FDA Inspection 1085190 - 2019-03-15
- FDA Inspection 1069417 - 2018-09-28
- FDA Inspection 1009607 - 2016-09-16
- FDA Inspection 1009606 - 2016-09-16
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