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FDA Inspection 841588 — Ambu A/S

Ambu A/S — FEI 3002806359

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

Facility

Other inspections at this facility

FDA data resources

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