FDA Inspection 1003949 — Bricon Technology GmbH

Bricon Technology GmbH — FEI 3004072627

The FDA completed an inspection of Bricon Technology GmbH on February 2, 2017 in Wurmlingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Wurmlingen (Germany)