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 3003166194.
Observations1
Issue DateDecember 16, 2013
StatusNo Warning Letter
Related Inspections10
Establishment Details
Firm
Medtronic MiniMed, Inc.
Location
Northridge, California, United States
FEI Number
3003166194
Product Type
Devices
Issue Date
December 16, 2013
Country
United States
Inspection History, 2014 to 2024
NAI4
VAI5
OAI1
NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.