FDA Inspection 1039589 — CG MEDTECH USA, INC.

CG MEDTECH USA, INC. — FEI 3009554293

The FDA completed an inspection of CG MEDTECH USA, INC. on Jan 4, 2018 in Irvine, CA. 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
Jan 4, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

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