FDA Inspection 586852 — CLEVERWAVE TECHNOLOGY INC

CLEVERWAVE TECHNOLOGY INC — FEI 3006291340

The FDA completed an inspection of CLEVERWAVE TECHNOLOGY INC on Apr 10, 2009 in Taoyuan 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
Apr 10, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Taoyuan City (Taiwan)

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