FDA Inspection 683833 — Bonasse Enterprises Co., Ltd.

Bonasse Enterprises Co., Ltd. — FEI 1000375210

The FDA completed an inspection of Bonasse Enterprises Co., Ltd. on Aug 20, 2010 in Chungli City. 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
Aug 20, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Chungli City (Taiwan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.