FDA inspection

Chongqing Xinfeng Medical Instruments Co., Ltd.: FDA inspection ending Sep 14, 2017

FDA inspection 1028487 · Voluntary Action Indicated (VAI) · Hechuan

Key facts

Inspection ID 1028487
Firm Chongqing Xinfeng Medical Instruments Co., Ltd.
FEI number 3005245626
Address 1st Floor, No. 8 Nanxi Group; Hechuan
City Hechuan
Country China
Fiscal year 2017
Inspection end date Sep 14, 2017
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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