FDA inspection

Hybio Pharmaceutical Co. Ltd (Site 1): FDA inspection ending Jun 26, 2015

FDA inspection 936556 · Voluntary Action Indicated (VAI) · Shenzhen

Key facts

Inspection ID 936556
Firm Hybio Pharmaceutical Co. Ltd (Site 1)
FEI number 3010165930
Address 37 Keji C, Str 2nd, Shenzhen Hi-Tech Ind
City Shenzhen
Country China
Fiscal year 2015
Inspection end date Jun 26, 2015
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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