FDA Inspection 1300106 — Alere San Diego Inc.
The FDA completed an inspection of Alere San Diego Inc. on Dec 10, 2025 in Pomona, CA. 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
- Dec 10, 2025
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Pomona, CA (United States)