FDA Inspection 710837 — Apneicare LLC

Apneicare LLC — FEI 3007799743

The FDA completed an inspection of Apneicare LLC on February 18, 2011 in Columbus, OH. 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
February 18, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)