FDA Inspection 896600 — Breathe Technologies, Inc.

Breathe Technologies, Inc. — FEI 3008778542

The FDA completed an inspection of Breathe Technologies, Inc. on Sep 22, 2014 in Irvine, CA. 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
Sep 22, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)