FDA Inspection
Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. – FDA Inspection, Dec 15, 2016
Record Details
This FDA Inspection record concerns Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd., with an inspection on December 15, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- December 15, 2016
- Product Type
- Drugs
View Company Profile
ID · d19297d6-d8f0-4335-8d79-6f09cd631a24
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 999895
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 28, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 7, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 23, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 1, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
- FDA Inspection 1216057 - 2023-07-28
- FDA Inspection 1077704 - 2018-12-07
- FDA Inspection 883329 - 2014-05-23
- FDA Inspection 672161 - 2010-07-01
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