FDA Inspection 1167825 — Flextronics International USA, Inc

Flextronics International USA, Inc — FEI 3011536730

The FDA completed an inspection of Flextronics International USA, Inc on Apr 19, 2022 in Buffalo Grove, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 19, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Buffalo Grove, IL (United States)

Citations

IDCFRDescription
317321 CFR 820.198(d)Evaluation, timeliness, identification
369621 CFR 820.100(b)Documentation
383721 CFR 820.25(b)Training records