FDA Inspection 1078710 — Cochlear Americas Inc.

Cochlear Americas Inc. — FEI 3005900820

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.