# Roche Diagnostics GmbH – FDA Inspection, Aug 29, 2019

Source: https://www.keypedia.com/records/fda_inspections/roche-diagnostics-gmbh/eb428e12-856a-41e1-9954-fd28c50f150f
Source feed: FDA_Inspections

> FDA inspection 1103444 of Roche Diagnostics GmbH, August 29, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 15 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1103444
- Company Name: Roche Diagnostics GmbH
- Inspection Date: 2019-08-29
- 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: 0

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- [FDA Inspection 1210168 - 2023-07-14](https://www.keypedia.com/records/fda_inspections/roche-diagnostics-gmbh/a0f27491-5e3a-4d48-8601-ea67f5698f18)
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- FDA Inspection 1057452 - 2018-04-19

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/roche-diagnostics-gmbh/a23249df-90f8-49fa-8a07-267a69157488

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