FDA Inspection 1152320 — Dexcom, Inc.

Dexcom, Inc. — FEI 3004753838

The FDA completed an inspection of Dexcom, Inc. on September 17, 2021 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 17, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures