# FDA Inspection 1040278 - STERIS Deutschland GmbH - February 08, 2018

Source: https://www.keypedia.com/records/fda_inspections/steris-deutschland-gmbh/1b4a06dd-cebc-43b0-ac7a-02df0ec3e984
Source feed: FDA_Inspections

> FDA Inspection 1040278 for STERIS Deutschland GmbH on February 08, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040278
- Company Name: STERIS Deutschland GmbH
- Inspection Date: 2018-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1193160 - 2022-11-04](https://www.keypedia.com/records/fda_inspections/steris-deutschland-gmbh/9c8925a1-6b18-49d3-95d6-606d90f8d454)
- [FDA Inspection 1040278 - 2018-02-08](https://www.keypedia.com/records/fda_inspections/steris-deutschland-gmbh/021c7cff-f4c8-45e8-91b6-5723500b180d)

Company: https://www.keypedia.com/companies/steris-deutschland-gmbh/c601bd47-c5a3-4270-bf64-c6cd4c239fea

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