FDA Inspection
Everyway Medical Instruments Co., LtdEveryway Medical Instruments Co., Ltd – FDA Inspection, May 16, 2019
Record Details
This FDA Inspection record concerns Everyway Medical Instruments Co., Ltd, with an inspection on May 16, 2019, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · 82f12a3c-e042-4c3d-9a74-4b68b910ec40
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1091287
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
Other FDA inspections of Everyway Medical Instruments Co., Ltd
3| Date | Classification | Office | Project area |
|---|---|---|---|
| August 12, 2026 | Not classified | Office of Inspections and Investigations | |
| August 29, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 20, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Everyway Medical Instruments Co., Ltd
- FDA Inspection 1335888 - 2026-08-12
- FDA Inspection 848654 - 2013-08-29
- FDA Inspection 709033 - 2011-01-20
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.