FDA Inspection 914434 — Alcon Grieshaber AG

Alcon Grieshaber AG — FEI 3003398873

The FDA completed an inspection of Alcon Grieshaber AG on February 19, 2015 in Schaffhausen. 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
February 19, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Schaffhausen (Switzerland)