FDA issued a Warning Letter to Alere San Diego, Inc. on 10/22/2012 as a result of this inspection.
483 Alere San Diego Jun 2012

483 Alere San Diego Jun 2012

Shaquenta Perkins FDA, Joey Quitania FDA, Scott Zika FDA$119.00 - Available Now

FDA investigators audited the Alere San Diego - San Diego, CA, United States facility and issued inspectional observations (via FDA 483) on 27 Jun 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 27 Jun 2012
  • Location: San Diego, United States
  • FEI: 1000125596
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