FDA Inspection
Zhejiang Huahai Pharmaceutical Co., Ltd.Zhejiang Huahai Pharmaceutical Co., Ltd. – FDA Inspection, Nov 18, 2016
Record Details
This FDA Inspection record concerns Zhejiang Huahai Pharmaceutical Co., Ltd., with an inspection on November 18, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 0b357083-d8c1-4b5b-9169-ab1f1c610575
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 993041
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Huahai Pharmaceutical Co., Ltd.
10| Date | Classification | Office | Project area |
|---|---|---|---|
| April 24, 2026 | Not classified | Office of Inspections and Investigations | |
| January 24, 2025 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 2, 2021 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 28, 2019 | Not classified | Office of Inspections and Investigations | |
| May 31, 2019 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Huahai Pharmaceutical Co., Ltd.
- FDA Inspection 1319736 - 2026-04-24
- FDA Inspection 1259818 - 2025-01-24
- FDA Inspection 1149252 - 2021-07-02
- FDA Inspection 1094941 - 2019-06-28
- FDA Inspection 1093250 - 2019-05-31
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