FDA Inspection 1094151 — Desyncra Operating Gmbh

Desyncra Operating Gmbh — FEI 3012377720

The FDA completed an inspection of Desyncra Operating Gmbh on May 16, 2019 in Bad Neuenahr-Ahrweiler. 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
May 16, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Bad Neuenahr-Ahrweiler (Germany)