FDA Inspection 1040047 — Dentsply Sirona Preventive

Dentsply Sirona Preventive — FEI 3002088145

The FDA completed an inspection of Dentsply Sirona Preventive on September 27, 2017 in York, PA. 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
September 27, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
York, PA (United States)