Medtronic MiniMed, Inc. Form 483 Details
Form 483Source: FDA record for this establishmentFDA 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 this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3003166194.
Medtronic MiniMed, Inc.
Northridge, California, United States
Issue DateDecember 16, 2013
FEI Number3003166194
CountryUnited States
Status
No Warning LetterProduct Type
Devices