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966611

Medtronic Neuromodulation — FEI 2182207

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 26, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Minneapolis, MN (United States)

Facility

Other inspections at this facility

  • 1206222 (VAI Fri May 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1187313 (VAI Thu Nov 03 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1153966 (NAI Thu Sep 09 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1108789 (VAI Thu Oct 17 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1102180 (NAI Tue Aug 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

Citations

IDCFRDescription
1472221 CFR 820.40Procedures not adequately established or maintained
312821 CFR 820.90(a)Nonconforming product control
313021 CFR 820.100(a)Lack of or inadequate procedures
419121 CFR 806.10(a)(1)Report of risk to health