FDA Inspection
Steris CorporationSteris Corporation – FDA Inspection, Oct 28, 2009
Record Details
This FDA Inspection record concerns Steris Corporation, with an inspection on October 28, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Steris Corporation
- Inspection Date
- October 28, 2009
- Product Type
- Devices
View Company Profile
ID · cb88a054-770d-41c8-9e6c-a83bfdf55c3a
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 625039
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Steris Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 16, 2026 | Not classified | New Orleans District Office | |
| June 9, 2017 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 4, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 21, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| October 27, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Steris Corporation
- FDA Inspection 1315862 - 2026-04-16
- FDA Inspection 1016465 - 2017-06-09
- FDA Inspection 950166 - 2015-12-04
- FDA Inspection 866506 - 2014-02-21
- FDA Inspection 751426 - 2011-10-27
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