FDA inspection

The Magstim Company Limited: FDA inspection ending Apr 30, 2015

FDA inspection 927906 · Voluntary Action Indicated (VAI) · Whitland

Key facts

Inspection ID 927906
Firm The Magstim Company Limited
FEI number 3002808356
Address Spring Gardens
City Whitland
Country United Kingdom
Fiscal year 2015
Inspection end date Apr 30, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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