# Shenzhen Hepalink Pharmaceutical Co., Ltd., Shenzhen, China – FDA Inspections

Source: https://www.keypedia.com/companies/shenzhen-hepalink-pharmaceutical-co-ltd/73ab214e-7ba7-4484-bce3-4bf799bfa729

> Inspection records and compliance data for Shenzhen Hepalink Pharmaceutical Co., Ltd. in Shenzhen. 5 FDA inspections on record, last inspected January 13, 2020.

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## Details

- Name: Shenzhen Hepalink Pharmaceutical Co., Ltd.
- FEI Number: 3002808210
- Business Operations: API MANUFACTURE, API/FDF ANALYTICAL TESTING
- Address Line 1: Songpingshan, 21 Langshan Road; Nanshan District
- City: Shenzhen
- Country Name: China
- Address: Songpingshan, 21 Langshan Road; Nanshan District, Shenzhen, China
- Country: China

## Related Documents

- FDA Inspection 1134048 - Shenzhen Hepalink Pharmaceutical Co., Ltd. - 2020-01-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2020
- FDA Inspection 988107 - Shenzhen Hepalink Pharmaceutical Co., Ltd. - 2016-06-16 — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2016
- FDA Inspection 823038 - Shenzhen Hepalink Pharmaceutical Co., Ltd. - 2013-01-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2013
- FDA Inspection 717785 - Shenzhen Hepalink Pharmaceutical Co., Ltd. - 2011-01-27 — classification: No Action Indicated (NAI), source: FDA, date: January 27, 2011
- FDA Inspection 556264 - Shenzhen Hepalink Pharmaceutical Co., Ltd. - 2008-11-26 — classification: No Action Indicated (NAI), source: FDA, date: November 26, 2008

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