# FDA Inspection 891424 - Steris Corporation Hopkins Facility - September 19, 2014

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation-hopkins-facility/80bb10f5-ef30-4061-8c19-a727776134f2
Source feed: FDA_Inspections

> FDA Inspection 891424 for Steris Corporation Hopkins Facility on September 19, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891424
- Company Name: Steris Corporation Hopkins Facility
- Inspection Date: 2014-09-19
- 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-hopkins-facility/bda59038-3a74-4e02-9bf4-d3a837e791d5

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