# Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd., Jinhua, China – FDA Inspections

Source: https://www.keypedia.com/companies/zhejiang-apeloa-kangyu-pharmaceutical-co-ltd/3fca869b-8499-4731-95c4-d6a48fb2cdb0

> Inspection records and compliance data for Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. in Jinhua. 5 FDA inspections on record, 2 Form 483s, last inspected July 28, 2023.

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## Details

- Name: Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
- FEI Number: 3003744129
- Business Operations: API MANUFACTURE, FDF MANUFACTURE
- Address Line 1: 333 Jiang South Rd, Hengdianzhen Dongyang
- City: Jinhua
- Country Name: China
- Address: 333 Jiang South Rd, Hengdianzhen Dongyang, Jinhua, China
- Country: China

## Related Documents

- [FDA Inspection 1216057 - Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. - 2023-07-28](https://www.keypedia.com/records/fda_inspections/zhejiang-apeloa-kangyu-pharmaceutical-co-ltd/59ccd325-677e-420a-b548-6dfbb9409922) — classification: No Action Indicated (NAI), source: FDA, date: July 28, 2023
- [FDA Inspection 1077704 - Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. - 2018-12-07](https://www.keypedia.com/records/fda_inspections/zhejiang-apeloa-kangyu-pharmaceutical-co-ltd/e4c63183-cb7f-41ef-ac53-3d4f36b4e191) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 7, 2018
- [FDA Inspection 999895 - Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. - 2016-12-15](https://www.keypedia.com/records/fda_inspections/zhejiang-apeloa-kangyu-pharmaceutical-co-ltd/d19297d6-d8f0-4335-8d79-6f09cd631a24) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 15, 2016
- EMA GMP - Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. - DE-NI-04-20141029 - 2014-11-21 — source: EMA, date: November 21, 2014
- FDA Inspection 883329 - Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. - 2014-05-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2014
- FDA Inspection 672161 - Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. - 2010-07-01 — classification: No Action Indicated (NAI), source: FDA, date: July 1, 2010

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