# FDA Inspection 601503 - Steris Corporation - July 29, 2009

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation/67b03b0e-c47b-44b8-8fd7-48b1e3701874
Source feed: FDA_Inspections

> FDA Inspection 601503 for Steris Corporation on July 29, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 601503
- Company Name: Steris Corporation
- Inspection Date: 2009-07-29
- Classification: Voluntary Action Indicated (VAI)
- 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/269007a3-44bb-40d4-ad7c-3ab87774c0d5

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