Home / Inspections / 1042301

FDA Inspection 1042301 — Veran Medical Technologies Inc

Veran Medical Technologies Inc — FEI 3007222345

The FDA completed an inspection of Veran Medical Technologies Inc on February 23, 2018 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
February 23, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
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))
  • 1077815 (VAI Thu Jan 31 2019 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