Source: FDA record for this establishment. FDA publishes inspections or enforcement actions for this establishment, listed further down this page, but we have not matched this particular Form 483 to a document or an inspection date FDA has released. It stays out of the default view for that reason. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 2182207.
Observations5
Issue DateJanuary 21, 2011
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
Medtronic Neuromodulation
Location
Minneapolis, Minnesota, United States
FEI Number
2182207
Product Type
Devices
Issue Date
January 21, 2011
Country
United States
Inspection History, 2013 to 2023
NAI3
VAI7
NAI means No Action Indicated. VAI means Voluntary Action Indicated.