FDA Inspection 1109312 — Bricon Technology GmbH

Bricon Technology GmbH — FEI 3004072627

The FDA completed an inspection of Bricon Technology GmbH on October 17, 2019 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
October 17, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Wurmlingen (Germany)