FDA inspection

MatOrtho Ltd: FDA inspection ending Oct 22, 2015

FDA inspection 949343 · Voluntary Action Indicated (VAI) · Leatherhead

Key facts

Inspection ID 949343
Firm MatOrtho Ltd
FEI number 3008985661
Address 19/20 Mole Business Park, Randalls Road
City Leatherhead
Country United Kingdom
Fiscal year 2016
Inspection end date Oct 22, 2015
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 10–99 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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