FDA Inspection 1078412 — Admedes GmbH

Admedes GmbH — FEI 3003956144

The FDA completed an inspection of Admedes GmbH on December 7, 2018 in Pforzheim. 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
December 7, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Pforzheim (Germany)