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FDA Inspection 790083 — Centurion Medical Products, LP

Centurion Medical Products, LP — FEI 1824619

The FDA completed an inspection of Centurion Medical Products, LP on June 29, 2012 in Howell, MI. 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, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Howell, MI (United States)

Facility

Other inspections at this facility

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  • 1100169 (NAI Tue Aug 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1061406 (NAI Tue Jun 26 2018 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))

Recent compliance actions

FDA data resources