# FDA Inspection 630421 - Steris Corporation Hopkins Facility - November 06, 2009

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation-hopkins-facility/eccded80-c2a2-44c0-9aba-6fb09b3ed4e2
Source feed: FDA_Inspections

> FDA Inspection 630421 for Steris Corporation Hopkins Facility on November 06, 2009. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 630421
- Company Name: Steris Corporation Hopkins Facility
- Inspection Date: 2009-11-06
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 891424 - 2014-09-19](https://www.keypedia.com/records/fda_inspections/steris-corporation-hopkins-facility/80bb10f5-ef30-4061-8c19-a727776134f2)
- [FDA Inspection 786100 - 2012-06-12](https://www.keypedia.com/records/fda_inspections/steris-corporation-hopkins-facility/9114ce74-9230-4408-b16c-1fad6096d818)
- [FDA Inspection 713862 - 2011-04-12](https://www.keypedia.com/records/fda_inspections/steris-corporation-hopkins-facility/aa28b979-7c78-4a0f-a055-7fcd1f0acf8e)

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