FDA Inspection 920920 — Anshi Pharmaceutical (Zhongshan) Inc.

Anshi Pharmaceutical (Zhongshan) Inc. — FEI 3006689272

The FDA completed an inspection of Anshi Pharmaceutical (Zhongshan) Inc. on March 20, 2015 in Zhongshan. 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
March 20, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Zhongshan (China)