FDA Inspection 644678 — Dexcom, Inc.

Dexcom, Inc. — FEI 3004753838

The FDA completed an inspection of Dexcom, Inc. on Feb 8, 2010 in San Diego, CA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Feb 8, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

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