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FDA Inspection 931956 — Alere San Diego, Inc.

Alere San Diego, Inc. — FEI 1000125596

The FDA completed an inspection of Alere San Diego, Inc. on June 5, 2015 in San Diego, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 5, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Facility

Other inspections at this facility

  • 1076303 (VAI Fri Jan 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 878268 (NAI Fri Jun 27 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 781860 (OAI Wed Jun 27 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 581906 (VAI Fri May 08 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources