FDA inspection

BONART CO. LTD.: FDA inspection ending Jul 17, 2014

FDA inspection 891962 · Voluntary Action Indicated (VAI) · KEELUNG, TAIPEI

Key facts

Inspection ID 891962
Firm BONART CO. LTD.
FEI number 3008981576
Address NO. 80, WUXAN STREET ANLE DISTRICT
City KEELUNG, TAIPEI
Country Taiwan
Fiscal year 2014
Inspection end date Jul 17, 2014
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No 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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