FDA Inspection 1078412 — Admedes GmbH

Admedes GmbH — FEI 3003956144

The FDA completed an inspection of Admedes GmbH on Dec 7, 2018 in Pforzheim. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 7, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Pforzheim (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.