FDA Inspection 1282062 — Jabil Tuttlingen Manufacturing GMBH

Jabil Tuttlingen Manufacturing GMBH — FEI 3017521423

The FDA completed an inspection of Jabil Tuttlingen Manufacturing GMBH on September 18, 2025 in Tuttlingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 18, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tuttlingen (Germany)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
322621 CFR 820.70(g)(1)Maintenance schedule, Lack of or inadequate schedule
326321 CFR 820.250(b)Sampling plans