FDA Inspection 734366 — BONART CO. LTD.
The FDA completed an inspection of BONART CO. LTD. on April 21, 2011 in KEELUNG, TAIPEI. 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
- KEELUNG, TAIPEI (Taiwan)