FDA Inspection
Steris CorporationSteris Corporation – FDA Inspection, Nov 6, 2009
Record Details
This FDA Inspection record concerns Steris Corporation, with an inspection on November 6, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Steris Corporation
- Inspection Date
- November 6, 2009
- Product Type
- Devices
View Company Profile
ID · 0fe0eed5-9b5d-4126-8c81-d9124f2dd337
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 617014
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
3- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.100(a)(1)Analysis of data/reports from data sources
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Steris Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 13, 2020 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 19, 2014 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 12, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 12, 2011 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Steris Corporation
- FDA Inspection 1120788 - 2020-03-13
- FDA Inspection 891420 - 2014-09-19
- FDA Inspection 775515 - 2012-06-12
- FDA Inspection 712327 - 2011-04-12
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