FDA Inspection 1246648 — Keronics LLC

Keronics LLC — FEI 3018380723

The FDA completed an inspection of Keronics LLC on Aug 9, 2024 in San Diego, 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
Aug 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)