FDA inspection

REMEDI CO., LTD.: FDA inspection ending Mar 17, 2023

FDA inspection 1199976 · No Action Indicated (NAI) · Chuncheon

Key facts

Inspection ID 1199976
Firm REMEDI CO., LTD.
FEI number 3013779985
Address 2f 69-14, Sakju-Ro 145beon-Gil
City Chuncheon
Country Korea (the Republic of)
Fiscal year 2023
Inspection end date Mar 17, 2023
Classification No Action Indicated (NAI)
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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