FDA Inspection
Tianjin Tianyao Pharmaceuticals Co., Ltd.Tianjin Tianyao Pharmaceuticals Co., Ltd. – FDA Inspection, Aug 24, 2017
Record Details
This FDA Inspection record concerns Tianjin Tianyao Pharmaceuticals Co., Ltd., with an inspection on August 24, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · d50a01d1-9785-46c1-ac1d-afb637f33e05
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1024734
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Tianjin Tianyao Pharmaceuticals Co., Ltd.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 13, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 24, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 2, 2016 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 5, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 17, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Tianjin Tianyao Pharmaceuticals Co., Ltd.
- FDA Inspection 1259925 - 2024-12-13
- FDA Inspection 1094116 - 2019-05-24
- FDA Inspection 983628 - 2016-09-02
- FDA Inspection 854729 - 2013-07-05
- FDA Inspection 672157 - 2010-06-17
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