# Steris Corporation – FDA Inspection, Oct 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation/cb88a054-770d-41c8-9e6c-a83bfdf55c3a
Source feed: FDA_Inspections

> FDA inspection 625039 of Steris Corporation, October 28, 2009. Classification: Official Action Indicated (OAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 625039
- Company Name: Steris Corporation
- Inspection Date: 2009-10-28
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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- [FDA Inspection 866506 - 2014-02-21](https://www.keypedia.com/records/fda_inspections/steris-corporation/d027ade8-6743-4be9-b6db-748154210261)
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Company: https://www.keypedia.com/companies/steris-corporation/9a86b47c-a3bd-4ea6-b89b-fc42e41f42e4

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
