# FDA Inspection 1282062 - Jabil Tuttlingen Manufacturing GMBH - September 18, 2025

Source: https://www.keypedia.com/records/fda_inspections/jabil-tuttlingen-manufacturing-gmbh/e0dead16-cea2-4570-99b9-e784f79db2b5
Source feed: FDA_Inspections

> FDA Inspection 1282062 for Jabil Tuttlingen Manufacturing GMBH on September 18, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1282062
- Company Name: Jabil Tuttlingen Manufacturing GMBH
- Inspection Date: 2025-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1282062 - 2025-09-18](https://www.keypedia.com/records/fda_inspections/jabil-tuttlingen-manufacturing-gmbh/2e3be7d3-41df-45c6-bd25-a70e45e62efc)
- [FDA Inspection 1282062 - 2025-09-18](https://www.keypedia.com/records/fda_inspections/jabil-tuttlingen-manufacturing-gmbh/b40b83bb-a5a7-4f02-a6d3-74d470845c38)
- [FDA Inspection 1282062 - 2025-09-18](https://www.keypedia.com/records/fda_inspections/jabil-tuttlingen-manufacturing-gmbh/883b6d38-450d-4cef-850a-e009e79a84e4)

Company: https://www.keypedia.com/companies/jabil-tuttlingen-manufacturing-gmbh/6b64e618-8a46-422d-af67-c29a3d4dba86

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