FDA Inspection 763596 — Ambu Inc.

Ambu Inc. — FEI 1121788

The FDA completed an inspection of Ambu Inc. on Jan 13, 2012 in Columbia, MD. 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
Jan 13, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia, MD (United States)

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