FDA Inspection 1220386 — Dexcom, Inc.

Dexcom, Inc. — FEI 3004753838

The FDA completed an inspection of Dexcom, Inc. on September 29, 2023 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 29, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)