FDA Inspection 1067094 — Garmin International, Inc.
The FDA completed an inspection of Garmin International, Inc. on Aug 23, 2018 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
- Aug 23, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Radiation Control and Health Safety Act
- Location
- Olathe, KS (United States)