Medtronic

Form 483

Minneapolis, Minnesota, United StatesFEI 3004097636Issued January 22, 2010

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed 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 it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3004097636.

Observations2

Issue DateJanuary 22, 2010

StatusNo Warning Letter

Related Inspections4

Establishment Details

Firm: Medtronic
Location: Minneapolis, Minnesota, United States
FEI Number: 3004097636
Product Type: Biologics
Issue Date: January 22, 2010
Country: United States

Inspection History, 2010 to 2016

NAI3

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Medtronic FDA Form 483, Minneapolis, Minnesota, January 22, 2010