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FDA Inspection
•Shenzhen Techdow Pharmaceutical Co., Ltd.•January 23, 2015

FDA Inspection 912579 - Shenzhen Techdow Pharmaceutical Co., Ltd. - January 23, 2015

Record Details

This FDA Inspection record concerns Shenzhen Techdow Pharmaceutical Co., Ltd., with an inspection on January 23, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Shenzhen Techdow Pharmaceutical Co., Ltd.
Inspection Date
January 23, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 13b4c043-24b6-4bfb-8965-314c4334ce61

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
912579
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Shenzhen Techdow Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
July 14, 2026Not classifiedOffice of Inspections and Investigations
September 17, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 15, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Shenzhen Techdow Pharmaceutical Co., Ltd.
  • FDA Inspection 1329698 - 2026-07-14
  • FDA Inspection 1107003 - 2019-09-17
  • FDA Inspection 776767 - 2012-03-15

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