FDA Inspection
Shandong Anhong Pharmaceutical Co., Ltd.Shandong Anhong Pharmaceutical Co., Ltd. – FDA Inspection, Feb 22, 2019
Record Details
This FDA Inspection record concerns Shandong Anhong Pharmaceutical Co., Ltd., with an inspection on February 22, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 8b8439c6-6656-45ee-aba1-007a022eb5f5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1081775
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Shandong Anhong Pharmaceutical Co., Ltd.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| September 2, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 13, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shandong Anhong Pharmaceutical Co., Ltd.
- FDA Inspection 983627 - 2016-09-02
- FDA Inspection 851827 - 2013-09-13
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