FDA Inspection 1037834 — Adcura Inc

Adcura Inc — FEI 3013758617

The FDA completed an inspection of Adcura Inc on December 12, 2017 in Minnetonka, MN. 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
December 12, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)