FDA Inspection 841588 — Ambu A/S

Ambu A/S — FEI 3002806359

The FDA completed an inspection of Ambu A/S on June 19, 2013 in Ballerup. 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
June 19, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ballerup (Denmark)