FDA issued a Warning Letter to Simpro on 8/17/2016 as a result of this inspection.
483 Simpro Jul 2016

483 Simpro Jul 2016

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FDA investigators audited the Simpro - Irving, TX, United States facility and issued inspectional observations (via FDA 483) on 07 Jul 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 07 Jul 2016
  • Location: Irving, United States
  • FEI: 3004485927
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