FDA Inspection 604345 — Kunshan Oriental Pharmaceutical Co., Ltd.

Kunshan Oriental Pharmaceutical Co., Ltd. — FEI 3005333852

The FDA completed an inspection of Kunshan Oriental Pharmaceutical Co., Ltd. on July 28, 2009 in Suzhou. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
July 28, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Suzhou (China)