FDA Inspection 1014987 — DentSply Sirona

DentSply Sirona — FEI 1419322

The FDA completed an inspection of DentSply Sirona on May 5, 2017 in Des Plaines, IL. 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
May 5, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Des Plaines, IL (United States)