FDA Inspection 777536 — Miracle-Ear, Inc.

Miracle-Ear, Inc. — FEI 2110592

The FDA completed an inspection of Miracle-Ear, Inc. on Apr 18, 2012 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
Apr 18, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Plymouth, MN (United States)