FDA Inspection
Lianyungang Runzhong Pharmaceutical Co., Ltd.Lianyungang Runzhong Pharmaceutical Co., Ltd. – FDA Inspection, Jul 28, 2011
Record Details
This FDA Inspection record concerns Lianyungang Runzhong Pharmaceutical Co., Ltd., with an inspection on July 28, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 28, 2011
- Product Type
- Drugs
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ID · 5666b439-3001-4032-b1b0-a3cf7ddd254d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 738641
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Lianyungang Runzhong Pharmaceutical Co., Ltd.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 26, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 27, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Lianyungang Runzhong Pharmaceutical Co., Ltd.
- FDA Inspection 1230851 - 2024-01-26
- FDA Inspection 1073786 - 2018-10-26
- FDA Inspection 873844 - 2014-03-27
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