# Shenzhen Techdow Pharmaceutical Co., Ltd. - Inspection Records

Source: https://www.keypedia.com/companies/shenzhen-techdow-pharmaceutical-co-ltd/0086e099-5a81-4022-b788-e1b105259f64

> Inspection records and compliance data for Shenzhen Techdow Pharmaceutical Co., Ltd. in Shenzhen. 4 FDA inspections on record, 1 Form 483, last inspected July 14, 2026.

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## Details

- Name: Shenzhen Techdow Pharmaceutical Co., Ltd.
- FEI Number: 3005599762
- Business Operations: API MANUFACTURE, FDF MANUFACTURE
- Address Line 1: 19 Gaoxinzhongyi Road, Nanshan
- City: Shenzhen
- Country Name: China
- Address: 19 Gaoxinzhongyi Road, Nanshan, Shenzhen, China
- Country: China

## Related Documents

- [FDA Inspection 1329698 - Shenzhen Techdow Pharmaceutical Co., Ltd. - 2026-07-14](https://www.keypedia.com/records/fda_inspections/shenzhen-techdow-pharmaceutical-co-ltd/f20cff9d-5ee0-438c-a695-0b38e4ec2037) — source: FDA, date: July 14, 2026
- FDA Inspection 1107003 - Shenzhen Techdow Pharmaceutical Co., Ltd. - 2019-09-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 17, 2019
- FDA Inspection 912579 - Shenzhen Techdow Pharmaceutical Co., Ltd. - 2015-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2015
- FDA Inspection 776767 - Shenzhen Techdow Pharmaceutical Co., Ltd. - 2012-03-15 — classification: No Action Indicated (NAI), source: FDA, date: March 15, 2012

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