FDA Inspection 1291732 — Hakko Co., Ltd.

Hakko Co., Ltd. — FEI 3002807220

The FDA completed an inspection of Hakko Co., Ltd. on November 13, 2025 in Chikuma. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 13, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Chikuma (Japan)

Citations

IDCFRDescription
333121 CFR 820.181DMR - not or inadequately maintained