FDA Inspection 997597 — Nemoto Kyorindo Co., Ltd.

Nemoto Kyorindo Co., Ltd. — FEI 3008918179

The FDA completed an inspection of Nemoto Kyorindo Co., Ltd. on Dec 15, 2016 in Kawaguchi. 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
Dec 15, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kawaguchi (Japan)

Citations

IDCFRDescription
319221 CFR 820.30(g)Design validation - user needs and intended uses

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.