FDA Inspection
Medtronic Navigation, Inc.Medtronic Navigation, Inc. – FDA Inspection, May 25, 2017
Record Details
This FDA Inspection record concerns Medtronic Navigation, Inc., with an inspection on May 25, 2017, issued by the Denver District Office, covering medical devices & rad health.
- Company
- Medtronic Navigation, Inc.
- Inspection Date
- May 25, 2017
- Product Type
- Medical Devices & Rad Health
- Office
- Denver District Office
View Company Profile
ID · 62f2d29b-f2eb-42e0-8eb0-160b3bbbe989
Inspection Facts
- Inspection number
- 1025685
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Medtronic Navigation, Inc.
14| Date | Classification | Office | Project area |
|---|---|---|---|
| August 27, 2025 | Not classified | Denver District Office | |
| February 9, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 29, 2021 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 30, 2019 | VAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| August 2, 2018 | Not classified | Denver District Office |
Other documents for Medtronic Navigation, Inc.
- FDA Inspection 1287072 - 2025-08-27
- FDA Inspection 1231178 - 2024-02-09
- FDA Inspection 1145034 - 2021-06-29
- FDA Inspection 1103549 - 2019-09-30
- FDA Inspection 1106068 - 2018-08-02
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.