Drug factory · FDA FEI 3005599762
Shenzhen Techdow Pharmaceutical Co., Ltd.
No. 19, Gaoxinzhongyi Road, Nanshan District, Shenzhen, China
Problems found, fixed voluntarily at FDA's last inspection, Sep 17, 2019.
Voluntary Action Indicated: inspectors found problems, but not serious enough for FDA to take action. The company is expected to fix them.
3 drug inspections on record since 2012: 2 with no problems, 1 with problems fixed voluntarily, 0 with FDA action.
What it does, for whom
| Drug | Role | For | NDC |
|---|---|---|---|
| Enoxaparin | Makes it and tests it | Hepalink USA Inc., Northstar Rx LLC., Sandoz Inc. | 81952-123, 81952-124, 81952-126 +18 |
| Heparin | Makes it and tests it | Hepalink USA Inc., McKesson Packaging Services Business Unit of McKesson Corporation, Northstar Rx LLC., Sandoz Inc. | 81952-111, 81952-112, 81952-113 +24 |
FDA inspection history
| Ended | Result | Program | Problems noted |
|---|---|---|---|
| Sep 17, 2019 | Problems found, fixed voluntarily | Drug Quality Assurance | — |
| Jan 23, 2015 | No problems found | Drug Quality Assurance | — |
| Mar 15, 2012 | No problems found | Drug Quality Assurance | — |
Registered with FDA for: analysis; manufacture.