FDA Inspection
Hangzhou Zhongmei Huadong Pharmaceutical Co., LtdHangzhou Zhongmei Huadong Pharmaceutical Co., Ltd – FDA Inspection, Sep 18, 2026
Record Details
This FDA Inspection record concerns Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd, with an inspection on September 18, 2026, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- September 18, 2026
- Product Type
- Human Drugs
View Company Profile
ID · e44708e7-3e03-4802-a6d2-f825b8255f90
Inspection Facts
- Inspection number
- 1341100
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
6| Date | Classification | Office | Project area |
|---|---|---|---|
| August 18, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 23, 2018 | 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 1217084 - 2023-08-18
- FDA Inspection 1064409 - 2018-08-23
- FDA Inspection 1006423 - 2017-02-28
- FDA Inspection 985170 - 2016-07-28
- FDA Inspection 880928 - 2014-05-02
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