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FDA Inspection 1061406 — Centurion Medical Products, LP

Centurion Medical Products, LP — FEI 1824619

The FDA completed an inspection of Centurion Medical Products, LP on June 26, 2018 in Howell, 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
June 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Howell, MI (United States)

Facility

Other inspections at this facility

  • 1168643 (NAI Tue Apr 05 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1100169 (NAI Tue Aug 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 944939 (VAI Mon Sep 21 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919616 (OAI Thu Mar 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 790083 (VAI Fri Jun 29 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources