FDA Inspection
Gyrus ACMI, Inc.Gyrus ACMI, Inc. – FDA Inspection, Dec 11, 2015
Record Details
This FDA Inspection record concerns Gyrus ACMI, Inc., with an inspection on December 11, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Gyrus ACMI, Inc.
- Inspection Date
- December 11, 2015
- Product Type
- Devices
View Company Profile
ID · f14d513c-5b14-43a3-91b7-d728755f766b
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 952450
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Gyrus ACMI, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| November 12, 2025 | Not classified | Minneapolis District Office | Compliance: Medical Devices |
| January 14, 2020 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 27, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 20, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 31, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Gyrus ACMI, Inc.
- FDA Inspection 1295532 - 2025-11-12
- FDA Inspection 1116173 - 2020-01-14
- FDA Inspection 1020250 - 2017-07-27
- FDA Inspection 920049 - 2015-03-20
- FDA Inspection 798492 - 2012-08-31
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.