FDA inspection

XIROS Ltd: FDA inspection ending Jun 29, 2017

FDA inspection 1016120 · Voluntary Action Indicated (VAI) · Leeds

Key facts

Inspection ID 1016120
Firm XIROS Ltd
FEI number 3013299874
Address Springfield House, White House Lane
City Leeds
Country United Kingdom
Fiscal year 2017
Inspection end date Jun 29, 2017
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
  • 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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