FDA Inspection 729255 — Bonart Co., Ltd.

Bonart Co., Ltd. — FEI 1000471278

The FDA completed an inspection of Bonart Co., Ltd. on April 21, 2011 in New Taipei City. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
April 21, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
New Taipei City (Taiwan)