FDA inspection

IMANI: FDA inspection ending Mar 22, 2023

FDA inspection 1200437 · Voluntary Action Indicated (VAI) · Yongin-Si

Key facts

Inspection ID 1200437
Firm IMANI
FEI number 3018159965
Address 147, Hwasan-Ro, Idong-Eup, Cheoin-Gu
City Yongin-Si
Country Korea (the Republic of)
Fiscal year 2023
Inspection end date Mar 22, 2023
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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