FDA Inspection 1131271 — Acclarent, Inc.

Acclarent, Inc. — FEI 3005172759

The FDA completed an inspection of Acclarent, Inc. on Sep 25, 2020 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 25, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.