FDA inspection

Plexus (Xiamen) Co Ltd: FDA inspection ending Jan 18, 2017

FDA inspection 1000877 · No Action Indicated (NAI) · Fujian

Key facts

Inspection ID 1000877
Firm Plexus (Xiamen) Co Ltd
FEI number 3006063136
Address 6 No Xiangxing 2 Rd Xiang Yu
City Fujian
Country China
Fiscal year 2017
Inspection end date Jan 18, 2017
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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