FDA inspection

ALPHANOX CO., LTD.: FDA inspection ending Dec 19, 2024

FDA inspection 1256802 · Voluntary Action Indicated (VAI) · Pyeongtaek

Key facts

Inspection ID 1256802
Firm ALPHANOX CO., LTD.
FEI number 3004941535
Address 154 Seotan-Ro, Seotan-Myeon
City Pyeongtaek
Country Korea (the Republic of)
Fiscal year 2025
Inspection end date Dec 19, 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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