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FDA Inspection 1040471 — Centurion Medical Products, LP

Centurion Medical Products, LP — FEI 3008403546

The FDA completed an inspection of Centurion Medical Products, LP on January 31, 2018 in Williamston, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 31, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Williamston, MI (United States)

Facility

Other inspections at this facility

  • 1199241 (NAI Fri Feb 10 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1108577 (OAI Fri Nov 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 987589 (VAI Wed Sep 28 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 855596 (VAI Mon Nov 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 825194 (NAI Tue Mar 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources