# FDA Inspection 1107003 - Shenzhen Techdow Pharmaceutical Co., Ltd. - September 17, 2019

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-techdow-pharmaceutical-co-ltd/3419961e-b7c2-4f22-af3c-ea7f69a9a742
Source feed: FDA_Inspections

> FDA inspection 1107003 of Shenzhen Techdow Pharmaceutical Co., Ltd., September 17, 2019. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1107003
- Company Name: Shenzhen Techdow Pharmaceutical Co., Ltd.
- Inspection Date: 2019-09-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- [FDA Inspection 1329698 - 2026-07-14](https://www.keypedia.com/records/fda_inspections/shenzhen-techdow-pharmaceutical-co-ltd/f20cff9d-5ee0-438c-a695-0b38e4ec2037)
- FDA Inspection 912579 - 2015-01-23
- FDA Inspection 776767 - 2012-03-15

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

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c