FDA Inspection
Steris Corporation Hopkins FacilitySteris Corporation Hopkins Facility – FDA Inspection, Nov 6, 2009
Record Details
This FDA Inspection record concerns Steris Corporation Hopkins Facility, with an inspection on November 6, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- November 6, 2009
- Product Type
- Devices
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ID · eccded80-c2a2-44c0-9aba-6fb09b3ed4e2
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 630421
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
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Other FDA inspections of Steris Corporation Hopkins Facility
3| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 |
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