FDA Inspection 1091206 — Gunze Limited
The FDA completed an inspection of Gunze Limited on Dec 13, 2018 in Ayabe. 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
- Dec 13, 2018
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Ayabe (Japan)