FDA Inspection 878906 — Tanita Corporation Of Akita Ltd.

Tanita Corporation Of Akita Ltd. — FEI 3008240972

The FDA completed an inspection of Tanita Corporation Of Akita Ltd. on Apr 17, 2014 in Daisen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Apr 17, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Daisen (Japan)

Citations

IDCFRDescription
1472221 CFR 820.40Procedures not adequately established or maintained
313021 CFR 820.100(a)Lack of or inadequate procedures
328621 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate

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