FDA inspection

JOOWON INNOVATION CO, LTD: FDA inspection ending Jan 18, 2024

FDA inspection 1227185 · Voluntary Action Indicated (VAI) · Cheonan

Key facts

Inspection ID 1227185
Firm JOOWON INNOVATION CO, LTD
FEI number 3012918760
Address 44 Sureteo1-Gil; Seobuk
City Cheonan
Country Korea (the Republic of)
Fiscal year 2024
Inspection end date Jan 18, 2024
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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