FDA Inspection 865961 — Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site)

Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site) — FEI 3003011617

The FDA completed an inspection of Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site) on December 13, 2013 in Hanzhong. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 13, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hanzhong (China)