FDA inspection

InTheSmart Co., Ltd.: FDA inspection ending Feb 12, 2019

FDA inspection 1085862 · No Action Indicated (NAI) · Jongro

Key facts

Inspection ID 1085862
Firm InTheSmart Co., Ltd.
FEI number 3014409527
Address Center For Medical Innovation (Cmi) Bldg., 71 Daehak-Ro
City Jongro
Country Korea (the Republic of)
Fiscal year 2019
Inspection end date Feb 12, 2019
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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