FDA Inspection 1063275 — SIVANTOS, INC.

SIVANTOS, INC. — FEI 3003291347

The FDA completed an inspection of SIVANTOS, INC. on Aug 7, 2018 in Plymouth, MN. 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
Aug 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Plymouth, MN (United States)