# STERIS Deutschland GmbH – FDA Inspection, Feb 8, 2018

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

> FDA inspection 1040278 of STERIS Deutschland GmbH, February 08, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 1193160 - 2022-11-04

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/thomas-a-peter/48a36892-cc03-42bb-8960-978d18f2147a)

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