# Steris Corporation Hopkins Facility – FDA Inspection, Jun 12, 2012

Source: https://www.keypedia.com/records/fda_inspections/steris-corporation-hopkins-facility/9114ce74-9230-4408-b16c-1fad6096d818
Source feed: FDA_Inspections

> FDA inspection 786100 of Steris Corporation Hopkins Facility, June 12, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 786100
- Company Name: Steris Corporation Hopkins Facility
- Inspection Date: 2012-06-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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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