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FDA Inspection 1118989 — Medtronic, Inc.

Medtronic, Inc. — FEI 2182208

The FDA completed an inspection of Medtronic, Inc. on February 4, 2020 in Mounds View, MN. 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
February 4, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mounds View, MN (United States)

Additional Details

Sponsor, Contract Research Organization

Facility

Other inspections at this facility

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  • 1217414 (NAI Fri Sep 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1052017 (OAI Mon May 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1029345 (NAI Wed Aug 30 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 963396 (NAI Mon Feb 29 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources