FDA Inspection 1055240 — Hunan Xiangyikang Pharmaceutical Co., Ltd.

Hunan Xiangyikang Pharmaceutical Co., Ltd. — FEI 3013723309

The FDA completed an inspection of Hunan Xiangyikang Pharmaceutical Co., Ltd. on May 18, 2018 in Yiyang. 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
May 18, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Yiyang (China)

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