FDA Inspection 1015620 — Curasan AG

Curasan AG — FEI 3003771570

The FDA completed an inspection of Curasan AG on May 12, 2017 in Kleinostheim. 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 12, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Kleinostheim (Germany)