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FDA Inspection 578776 — Primus Corporation

Primus Corporation — FEI 1931251

The FDA completed an inspection of Primus Corporation on April 15, 2009 in Kansas City, MO. 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
April 15, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Kansas City, MO (United States)

Facility

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  • 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))
  • 912071 (NAI Fri Jan 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources