FDA Inspection 1017656 — Tanita Corporation
The FDA completed an inspection of Tanita Corporation on Jun 8, 2017 in Itabashi. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 8, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Itabashi (Japan)