FDA issued a Warning Letter to LumiQuick Diagnostics Inc. on 4/1/2014 for a later inspection.
483 LumiQuick Diagnostics Dec 2012

483 LumiQuick Diagnostics Dec 2012

Timothy Grome FDA$119.00 - Available Now

FDA investigators audited the LumiQuick Diagnostics - Santa Clara, CA, United States facility and issued 7 inspectional observations (via FDA 483) on 07 Dec 2012.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 7
  • Inspection end: 07 Dec 2012
  • Location: Santa Clara, United States
  • FEI: 3005984081
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