FDA Inspection 927100 — Shandong Keyuan Pharmaceutical Co., Ltd.

Shandong Keyuan Pharmaceutical Co., Ltd. — FEI 3007607025

The FDA completed an inspection of Shandong Keyuan Pharmaceutical Co., Ltd. on Apr 10, 2015 in Jinan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 10, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jinan (China)