FDA Inspection
Jabil Tuttlingen Manufacturing GMBHJabil Tuttlingen Manufacturing GMBH – FDA Inspection, Sep 18, 2025
Record Details
This FDA Inspection record concerns Jabil Tuttlingen Manufacturing GMBH, with an inspection on September 18, 2025, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Inspection Date
- September 18, 2025
- Product Type
- Medical Devices & Rad Health
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ID · 2e3be7d3-41df-45c6-bd25-a70e45e62efc
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1282062
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
- 21 CFR 820.250(b)Sampling plans
- 21 CFR 820.100(a)Lack of or inadequate procedures
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