FDA Inspection 1222682 — Kessel Medical

Kessel Medical — FEI 3025664014

The FDA completed an inspection of Kessel Medical on Nov 6, 2023 in Vero Beach, 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
Nov 6, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Vero Beach, FL (United States)