FDA Inspection 1095299 — Tianjin Kingyork Pharmaceuticals Co., Ltd

Tianjin Kingyork Pharmaceuticals Co., Ltd — FEI 3013844768

The FDA completed an inspection of Tianjin Kingyork Pharmaceuticals Co., Ltd on May 31, 2019 in Tianjin. 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 31, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tianjin (China)

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