FDA Inspection 672161 — Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.

Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. — FEI 3003744129

The FDA completed an inspection of Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. on July 1, 2010 in Jinhua. 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
July 1, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jinhua (China)