FDA Inspection 1221144 — Garmin International, Inc.

Garmin International, Inc. — FEI 1000500214

The FDA completed an inspection of Garmin International, Inc. on Oct 18, 2023 in Olathe, KS. 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
Oct 18, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Olathe, KS (United States)