FDA Inspection 1060729 — Yiling Pharmaceutical Ltd.

Yiling Pharmaceutical Ltd. — FEI 3011640199

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.