FDA inspection

Alere San Diego Inc.: FDA inspection ending Dec 10, 2025

FDA inspection 1300106 · No Action Indicated (NAI) · Pomona, CA

Key facts

Inspection ID 1300106
Firm Alere San Diego Inc.
FEI number 2020952
Address 829 Towne Center Dr
City Pomona
State CA
ZIP 91767
Country United States
Fiscal year 2026
Inspection end date Dec 10, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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