FDA Inspection 961048 — Trokamed GmbH

Trokamed GmbH — FEI 3004595684

The FDA completed an inspection of Trokamed GmbH on February 19, 2016 in Geisingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 19, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Geisingen (Germany)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation