# FDA Inspection 891420 - Steris Corporation - September 19, 2014

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation/b047ab59-7a7a-4d30-b798-1d5a230d0398
Source feed: FDA_Inspections

> FDA Inspection 891420 for Steris Corporation on September 19, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891420
- Company Name: Steris Corporation
- Inspection Date: 2014-09-19
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/steris-corporation/e8aec574-95a0-48ab-9dbb-c2a8884ec770

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