# FDA Inspection 802103 - Steris Corporation - Distribution Center - October 04, 2012

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation-distribution-center/d6ce9e95-d03d-4521-a750-860eb1b6b53a
Source feed: FDA_Inspections

> FDA Inspection 802103 for Steris Corporation - Distribution Center on October 04, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 802103
- Company Name: Steris Corporation - Distribution Center
- Inspection Date: 2012-10-04
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/steris-corporation-distribution-center/ca1eb8de-9ec1-419c-8f07-3c2919859a79

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