FDA Inspection
Shenzhen Techdow Pharmaceutical Co., Ltd.Shenzhen Techdow Pharmaceutical Co., Ltd. – FDA Inspection, Mar 27, 2018
Record Details
This FDA Inspection record concerns Shenzhen Techdow Pharmaceutical Co., Ltd., with an inspection on March 27, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- March 27, 2018
- Product Type
- Human Drugs
View Company Profile
ID · 7042ce74-a401-4cae-971a-adbdde77ec5a
Inspection Facts
- Inspection number
- 1050101
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Shenzhen Techdow Pharmaceutical Co., Ltd.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 14, 2026 | Not classified | Office of Inspections and Investigations | |
| September 17, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 23, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 15, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Shenzhen Techdow Pharmaceutical Co., Ltd.
- FDA Inspection 1329698 - 2026-07-14
- FDA Inspection 1107003 - 2019-09-17
- FDA Inspection 912579 - 2015-01-23
- FDA Inspection 776767 - 2012-03-15
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