FDA Inspection 802637 — Novocure, Inc

Novocure, Inc — FEI 3009306483

The FDA completed an inspection of Novocure, Inc on Oct 10, 2012 in Portsmouth, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 10, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Portsmouth, NH (United States)