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FDA Inspection 1077815 — Veran Medical Technologies Inc

Veran Medical Technologies Inc — FEI 3007222345

The FDA completed an inspection of Veran Medical Technologies Inc on January 31, 2019 in Saint Louis, MO. 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
January 31, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Saint Louis, MO (United States)

Facility

Other inspections at this facility

  • 1198214 (VAI Thu Feb 23 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1147930 (NAI Thu Jul 29 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1042301 (VAI Fri Feb 23 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 912700 (NAI Wed Feb 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 677305 (NAI Wed Aug 25 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources