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FDA Inspection
•Shenzhen Techdow Pharmaceutical Co., Ltd.•September 17, 2019

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

Record Details

This FDA Inspection record concerns Shenzhen Techdow Pharmaceutical Co., Ltd., with an inspection on September 17, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Shenzhen Techdow Pharmaceutical Co., Ltd.
Inspection Date
September 17, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 3419961e-b7c2-4f22-af3c-ea7f69a9a742

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1107003
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
January 23, 2015NAICenter 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 912579 - 2015-01-23
  • FDA Inspection 776767 - 2012-03-15

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