FDA Inspection 955259 — Leisegang Feinmechanick-Optik GmbH

Leisegang Feinmechanick-Optik GmbH — FEI 3002807462

The FDA completed an inspection of Leisegang Feinmechanick-Optik GmbH on December 10, 2015 in Berlin. 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
December 10, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Berlin (Germany)