FDA Inspection 1049441 — Avent Inc

Avent Inc — FEI 3014274845

The FDA completed an inspection of Avent Inc on Apr 5, 2018 in Fort Lauderdale, FL. 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
Apr 5, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Fort Lauderdale, FL (United States)