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FDA Inspection 912071 — Primus Corporation

Primus Corporation — FEI 1931251

The FDA completed an inspection of Primus Corporation on January 30, 2015 in Kansas City, MO. 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 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kansas City, MO (United States)

Facility

Other inspections at this facility

  • 1180790 (NAI Mon Sep 26 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1154252 (NAI Fri Sep 17 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1117396 (OAI Thu Feb 06 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1064644 (OAI Thu Sep 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 783015 (VAI Fri May 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources