FDA Inspection 894791 — Moor Instruments Ltd

Moor Instruments Ltd — FEI 1000279065

The FDA completed an inspection of Moor Instruments Ltd on August 21, 2014 in Axminster. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 21, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Axminster (United Kingdom)