FDA Inspection 1060729 — Yiling Pharmaceutical Ltd.

Yiling Pharmaceutical Ltd. — FEI 3011640199

The FDA completed an inspection of Yiling Pharmaceutical Ltd. on June 15, 2018 in Shijiazhuang. 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
June 15, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shijiazhuang (China)