FDA Inspection 944716 — Medart A /S

Medart A /S — FEI 3005616124

The FDA completed an inspection of Medart A /S on September 24, 2015 in Hvidovre. 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
September 24, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Hvidovre (Denmark)