# Jabil Tuttlingen Manufacturing GMBH – FDA Inspection, Sep 18, 2025

Source: https://www.keypedia.com/records/fda_inspections/jabil-tuttlingen-manufacturing-gmbh/2e3be7d3-41df-45c6-bd25-a70e45e62efc
Source feed: FDA_Inspections

> FDA inspection 1282062 of Jabil Tuttlingen Manufacturing GMBH, September 18, 2025. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1282062
- Company Name: Jabil Tuttlingen Manufacturing GMBH
- Inspection Date: 2025-09-18
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 3

## Related Officers

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

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

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8