FDA Inspection 993216 — Spiraltech Dental Implants

Spiraltech Dental Implants — FEI 3012190987

The FDA completed an inspection of Spiraltech Dental Implants on Oct 20, 2016 in Chicago, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 20, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Chicago, IL (United States)