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FDA Inspection 1173562 — Cordis US Corp

Cordis US Corp — FEI 1016427

The FDA completed an inspection of Cordis US Corp on June 29, 2022 in Miami Lakes, FL. 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
June 29, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Miami Lakes, FL (United States)

Facility

Other inspections at this facility

  • 1323302 (NAI Tue Jun 09 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037525 (VAI Fri Jan 12 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 979906 (NAI Wed Jul 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 983423 (NAI Thu Mar 31 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 923766 (NAI Fri May 08 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources