FDA Inspection 564941 — Avent, Inc.

Avent, Inc. — FEI 3006646024

The FDA completed an inspection of Avent, Inc. on Feb 4, 2009 in Tucson, AZ. 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
Feb 4, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Tucson, AZ (United States)

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