# FDA Inspection 582973 - Steris - May 06, 2009

Source: https://www.keypedia.com/records/fda_inspections/steris/96a5a074-6c0c-4244-9ceb-fb5ba3f8c05a
Source feed: FDA_Inspections

> FDA Inspection 582973 for Steris on May 06, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 582973
- Company Name: Steris
- Inspection Date: 2009-05-06
- 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/6e20da70-37c0-4dc7-8e0c-9a2c5e589637

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