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FDA Inspection 1028385 — Genesis Biosystems, Inc

Genesis Biosystems, Inc — FEI 3003427273

The FDA completed an inspection of Genesis Biosystems, Inc on August 31, 2017 in Lewisville, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 31, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Lewisville, TX (United States)

Facility

Other inspections at this facility

  • 1195256 (VAI Mon Jan 09 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928343 (OAI Mon Jun 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 908043 (OAI Tue Dec 16 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 838279 (NAI Thu Jun 27 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources