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FDA Inspection 912579 — Shenzhen Techdow Pharmaceutical Co., Ltd.

Shenzhen Techdow Pharmaceutical Co., Ltd. — FEI 3005599762

The FDA completed an inspection of Shenzhen Techdow Pharmaceutical Co., Ltd. on January 23, 2015 in Shenzhen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 23, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shenzhen (China)

Facility

Other inspections at this facility

  • 1107003 (VAI Tue Sep 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 776767 (NAI Thu Mar 15 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources