FDA Inspection
Stryker Ireland, Ltd., Instruments DivisionStryker Ireland, Ltd., Instruments Division – FDA Inspection, Apr 19, 2018
Record Details
This FDA Inspection record concerns Stryker Ireland, Ltd., Instruments Division, with an inspection on April 19, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- April 19, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · d0ad0024-bf76-4464-a301-6fad740c9dc1
Inspection Facts
- Inspection number
- 1052438
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Stryker Ireland, Ltd., Instruments Division
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 25, 2024 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stryker Ireland, Ltd., Instruments Division
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.