FDA Inspection 883393 — Intersect ENT, Inc.

Intersect ENT, Inc. — FEI 3008301917

The FDA completed an inspection of Intersect ENT, Inc. on June 27, 2014 in Menlo Park, CA. 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
June 27, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Menlo Park, CA (United States)

Additional Details

Postmarket Audit Inspections