Medtronic Vascular, Inc. Form 483 Details
Form 483Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3005364322.
Medtronic Vascular, Inc.
Santa Rosa, California, United States
Issue DateSeptember 04, 2013
FEI Number3005364322
CountryUnited States
Status
No Warning LetterProduct Type
Devices