FDA Inspection 988493 — TEKNO MEDICAL OPTIK-CHIRURGIE GMBH

TEKNO MEDICAL OPTIK-CHIRURGIE GMBH — FEI 3002808335

The FDA completed an inspection of TEKNO MEDICAL OPTIK-CHIRURGIE GMBH on Jul 6, 2016 in Tuttlingen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)