FDA Inspection 860088 — Piezosurgery Inc

Piezosurgery Inc — FEI 3005282635

The FDA completed an inspection of Piezosurgery Inc on December 16, 2013 in Hilliard, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 16, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hilliard, OH (United States)