FDA Inspection 961487 — Novastep

Novastep — FEI 3010673777

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