FDA Inspection 1043597 — Spiraltech Dental Implants

Spiraltech Dental Implants — FEI 3012190987

The FDA completed an inspection of Spiraltech Dental Implants on Feb 22, 2018 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 22, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Chicago, IL (United States)