FDA inspection

CIMILRE CO., LTD.: FDA inspection ending Mar 21, 2019

FDA inspection 1090257 · No Action Indicated (NAI) · Cheonan-Si

Key facts

Inspection ID 1090257
Firm CIMILRE CO., LTD.
FEI number 3013561139
Address 97-14 Dongnam-Gu, Seongnam-Ro, Mokcheon-Eup
City Cheonan-Si
Country Korea (the Republic of)
Fiscal year 2019
Inspection end date Mar 21, 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
  • 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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