FDA Inspection 1078710 — Cochlear Americas Inc.

Cochlear Americas Inc. — FEI 3005900820

The FDA completed an inspection of Cochlear Americas Inc. on November 28, 2018 in Lone Tree, CO. 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
November 28, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lone Tree, CO (United States)