FDA Inspection
Stryker CorporationStryker Corporation – FDA Inspection, Oct 8, 2014
Record Details
This FDA Inspection record concerns Stryker Corporation, with an inspection on October 8, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Stryker Corporation
- Inspection Date
- October 8, 2014
- Product Type
- Devices
View Company Profile
ID · 92c57467-045e-4ac2-a797-b3600c4c8931
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 896766
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 806.10(a)(1)Report of risk to health
- 21 CFR 820.198(c)Investigation of device failures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Stryker Corporation
7| Date | Classification | Office | Project area |
|---|---|---|---|
| November 21, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 25, 2018 | Not classified | San Francisco District Office | |
| August 25, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 18, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 14, 2012 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Stryker Corporation
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.