FDA inspection

CTL BIOTEC: FDA inspection ending Jun 19, 2025

FDA inspection 1280952 · No Action Indicated (NAI) · Daegu

Key facts

Inspection ID 1280952
Firm CTL BIOTEC
FEI number 3025602479
Address Dalseo, Suite 410; Seongseo-Ro 329
City Daegu
Country Korea (the Republic of)
Fiscal year 2025
Inspection end date Jun 19, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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