FDA inspection

Chongqing Kanghua Ruiming S&T Co., Ltd.: FDA inspection ending Sep 5, 2019

FDA inspection 1107000 · Voluntary Action Indicated (VAI) · Chongqing

Key facts

Inspection ID 1107000
Firm Chongqing Kanghua Ruiming S&T Co., Ltd.
FEI number 3011442035
Address 1 Road, Tongjiaxi Industrial Park, Beibei
City Chongqing
Country China
Fiscal year 2019
Inspection end date Sep 5, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None 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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