FDA Inspection 761033 — Mytech Technology Co., Ltd.

Mytech Technology Co., Ltd. — FEI 3003876756

The FDA completed an inspection of Mytech Technology Co., Ltd. on Dec 9, 2011 in Xin Bei Shi. 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
Dec 9, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Xin Bei Shi (Taiwan)

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