FDA issued a Warning Letter to Alere San Diego, Inc. on 10/22/2012 for a previous inspection.
483 Alere San Diego Jun 2015

483 Alere San Diego Jun 2015

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FDA investigators audited the Alere San Diego - San Diego, CA, United States facility and issued inspectional observations (via FDA 483) on 05 Jun 2015.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 05 Jun 2015
  • Location: San Diego, United States
  • FEI: 1000125596
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