FDA Inspection 711358 — Admedes GmbH

Admedes GmbH — FEI 3003956144

The FDA completed an inspection of Admedes GmbH on March 2, 2011 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
March 2, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Pforzheim (Germany)

Additional Details

Postmarket Audit Inspections