FDA Inspection
Hangzhou Zhongmei Huadong Pharmaceutical Co., LtdHangzhou Zhongmei Huadong Pharmaceutical Co., Ltd – FDA Inspection, Aug 23, 2018
Record Details
This FDA Inspection record concerns Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd, with an inspection on August 23, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- August 23, 2018
- Product Type
- Drugs
View Company Profile
ID · 31479e24-41fa-4d66-ba23-c026eff9681c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1064409
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 18, 2026 | Not classified | Office of Inspections and Investigations | |
| August 18, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 28, 2017 | Not classified | Office of Inspections and Investigations | |
| July 28, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 2, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
- FDA Inspection 1341100 - 2026-09-18
- FDA Inspection 1217084 - 2023-08-18
- FDA Inspection 1006423 - 2017-02-28
- FDA Inspection 985170 - 2016-07-28
- FDA Inspection 880928 - 2014-05-02
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