FDA inspection

Plexus Corporation: FDA inspection ending Apr 13, 2018

FDA inspection 1049509 · Voluntary Action Indicated (VAI) · Buffalo Grove, IL

Key facts

Inspection ID 1049509
Firm Plexus Corporation
FEI number 3004105270
Address 2400 Millbrook Dr Ste A
City Buffalo Grove
State IL
ZIP 60089
Country United States
Fiscal year 2018
Inspection end date Apr 13, 2018
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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