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FDA Inspection 998373 — Midmark Corporation

Midmark Corporation — FEI 1523530

The FDA completed an inspection of Midmark Corporation on December 9, 2016 in Versailles, OH. 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
December 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Versailles, OH (United States)

Facility

Other inspections at this facility

  • 1048753 (VAI Mon Apr 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 880282 (VAI Mon Jun 09 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 790449 (VAI Thu Jun 28 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 742849 (OAI Mon Sep 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources