FDA Inspection
Shanghai SynTheAll Pharmaceutical Co., Ltd.Shanghai SynTheAll Pharmaceutical Co., Ltd. – FDA Inspection, Nov 30, 2018
Record Details
This FDA Inspection record concerns Shanghai SynTheAll Pharmaceutical Co., Ltd., with an inspection on November 30, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- November 30, 2018
- Product Type
- Human Drugs
View Company Profile
ID · a1f25176-dd9b-44dd-842e-373052db9e6f
Inspection Facts
- Inspection number
- 1075148
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Shanghai SynTheAll Pharmaceutical Co., Ltd.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 25, 2025 | Not classified | Office of Inspections and Investigations | |
| July 19, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 8, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 17, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 15, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shanghai SynTheAll Pharmaceutical Co., Ltd.
- FDA Inspection 1268173 - 2025-04-25
- FDA Inspection 1063500 - 2018-07-19
- FDA Inspection 969770 - 2016-04-08
- FDA Inspection 890518 - 2014-07-17
- FDA Inspection 846042 - 2013-08-15
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