FDA Inspection 961487 — Novastep

Novastep — FEI 3010673777

The FDA completed an inspection of Novastep on Feb 4, 2016 in Rennes. 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
Feb 4, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rennes (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.