FDA Inspection 893459 — Bonart Co., Ltd.
The FDA completed an inspection of Bonart Co., Ltd. on July 22, 2014 in New Taipei City. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 22, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- New Taipei City (Taiwan)