Medtronic Puerto Rico Operations Co.: FDA Inspections

25 inspections from Dec 12, 2008 to Mar 14, 2025, newest first. Showing 1 to 25.

What this list covers: FDA records filed under the name "Medtronic Puerto Rico Operations Co." and its spelling variant "Medtronic Puerto Rico Operations".

Back to the Medtronic Puerto Rico Operations Co. profile

DateSiteProductClassificationFEI
Mar 14, 2025Juncos, PRDevicesNo Action Indicated (NAI)3004369318
Oct 25, 2019Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
May 31, 2019Humacao, PRDevicesVoluntary Action Indicated (VAI)2647346
Feb 21, 2019Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
May 15, 2018Juncos, PRDevicesNo Action Indicated (NAI)3004369318
Aug 29, 2017Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
Jun 2, 2017Villalba, PRDevicesNo Action Indicated (NAI)2649622
Mar 31, 2017Humacao, PRDevicesVoluntary Action Indicated (VAI)2647346
Feb 17, 2017Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
Jun 14, 2016Villalba, PRDevicesNo Action Indicated (NAI)2649622
Apr 28, 2016Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
Nov 19, 2014Juncos, PRDevicesNo Action Indicated (NAI)3004369318
Jun 3, 2014Villalba, PRDevicesNo Action Indicated (NAI)2649622
Oct 25, 2013Juncos, PRDevicesNo Action Indicated (NAI)3004369318
Jul 16, 2013Humacao, PRDevicesNo Action Indicated (NAI)2647346
Aug 24, 2012Juncos, PRDevicesNo Action Indicated (NAI)3004369318
Nov 9, 2011Juncos, PRDevicesNo Action Indicated (NAI)3004369318
May 20, 2011Villalba, PRDevicesVoluntary Action Indicated (VAI)2649622
May 13, 2011Humacao, PRDevicesVoluntary Action Indicated (VAI)2647346
May 11, 2011Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
Jul 27, 2010Humacao, PRDevicesVoluntary Action Indicated (VAI)2647346
May 14, 2010Villalba, PRDevicesVoluntary Action Indicated (VAI)2649622
Mar 10, 2010Juncos, PRDevicesVoluntary Action Indicated (VAI)3004369318
Dec 15, 2008Juncos, PRDevicesOfficial Action Indicated (OAI)3004369318
Dec 12, 2008Villalba, PRDevicesNo Action Indicated (NAI)2649622

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.