FDA inspection

PLEXUS CORP. (UK) LIMITED: FDA inspection ending Sep 20, 2018

FDA inspection 1076071 · Voluntary Action Indicated (VAI) · Kelso

Key facts

Inspection ID 1076071
Firm PLEXUS CORP. (UK) LIMITED
FEI number 3008754394
Address Pinnacle Hill, Pinnacle hill Industrial Estate
City Kelso
Country United Kingdom
Fiscal year 2018
Inspection end date Sep 20, 2018
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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