FDA Inspection 894791 — Moor Instruments Ltd

Moor Instruments Ltd — FEI 1000279065

The FDA completed an inspection of Moor Instruments Ltd on Aug 21, 2014 in Axminster. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection details

Classification
Official Action Indicated (OAI)
End Date
Aug 21, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Axminster (United Kingdom)

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