FDA issued a Warning Letter to Ventlab LLC on 7/2/2014 for a previous inspection.
483 Ventlab Mar 2016

483 Ventlab Mar 2016

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FDA investigators audited the Ventlab - Grand Rapids, MI, United States facility and issued 1 inspectional observation (via FDA 483) on 02 Mar 2016.

Product details

  • Category: Medical Devices & Rad Health
  • Number of Observations: 1
  • Inspection end: 02 Mar 2016
  • Location: Grand Rapids, United States
  • FEI: 2246980
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