FDA Inspection 866095 — Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant)

Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant) — FEI 3010728912

The FDA completed an inspection of Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant) on December 20, 2013 in Wenzhou. 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
December 20, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wenzhou (China)