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FDA Inspection 855809 — Cochlear Americas Inc.

Cochlear Americas Inc. — FEI 3005900820

The FDA completed an inspection of Cochlear Americas Inc. on October 22, 2013 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
October 22, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lone Tree, CO (United States)

Facility

Other inspections at this facility

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  • 1078710 (NAI Wed Nov 28 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1042149 (OAI Thu Feb 22 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 849948 (NAI Wed Sep 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 582805 (NAI Tue May 12 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources