FDA inspection

Bistos Co Ltd: FDA inspection ending Nov 7, 2019

FDA inspection 1113055 · No Action Indicated (NAI) · Yongin

Key facts

Inspection ID 1113055
Firm Bistos Co Ltd
FEI number 3006179052
Address 7th Floor, A Bldg, Woolim Lions Valley 5, 144-3, Sangdaewon-Dong, Jungwon-Gu
City Yongin
Country Korea (the Republic of)
Fiscal year 2020
Inspection end date Nov 7, 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

Browse all FDA inspections