FDA Inspection 1253980 — JMS Co., Ltd.

JMS Co., Ltd. — FEI 1000162947

The FDA completed an inspection of JMS Co., Ltd. on Oct 21, 2024 in Hiroshima. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 21, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Hiroshima (Japan)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures

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