FDA inspection

PLEXUS CORP. (UK) LIMITED: FDA inspection ending May 30, 2024

FDA inspection 1245333 · No Action Indicated (NAI) · Kelso

Key facts

Inspection ID 1245333
Firm PLEXUS CORP. (UK) LIMITED
FEI number 3008754394
Address Lee Forbes Way
City Kelso
Country United Kingdom
Fiscal year 2024
Inspection end date May 30, 2024
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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