FDA inspection

Hankook Latex Gongup Co., Ltd.: FDA inspection ending Apr 27, 2000

FDA inspection 26071 · No Action Indicated (NAI) · Chunchon

Key facts

Inspection ID 26071
Firm Hankook Latex Gongup Co., Ltd.
FEI number 3002260664
Address 622-1 Hupyeong-dong
City Chunchon
Fiscal year 2000
Inspection end date Apr 27, 2000
Classification No Action Indicated (NAI)
Project area Compliance: Med 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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