FDA Inspection 936556 — Hybio Pharmaceutical Co. Ltd (Site 1)

Hybio Pharmaceutical Co. Ltd (Site 1) — FEI 3010165930

The FDA completed an inspection of Hybio Pharmaceutical Co. Ltd (Site 1) on Jun 26, 2015 in Shenzhen. 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 26, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shenzhen (China)