FDA Inspection 964550 — Mahe Medical Gmbh

Mahe Medical Gmbh — FEI 3003002738

The FDA completed an inspection of Mahe Medical Gmbh on March 4, 2016 in Emmingen-Liptingen. 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
March 4, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Emmingen-Liptingen (Germany)