FDA Inspection 903415 — Alere San Diego Inc.
The FDA completed an inspection of Alere San Diego Inc. on Oct 29, 2014 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
- Oct 29, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Pomona, CA (United States)