FDA inspection

Geon Corporation: FDA inspection ending Jul 17, 2014

FDA inspection 890299 · Voluntary Action Indicated (VAI) · Zhang Hua Xian

Key facts

Inspection ID 890299
Firm Geon Corporation
FEI number 3005479955
Address No. 12, Gung Ye Road,, Hsi Hu
City Zhang Hua Xian
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

  • None 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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