FDA Inspection 1082757 — Intersect ENT, Inc.

Intersect ENT, Inc. — FEI 3008301917

The FDA completed an inspection of Intersect ENT, Inc. on March 6, 2019 in Menlo Park, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 6, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Menlo Park, CA (United States)