FDA Inspection 564941 — Avent, Inc.

Avent, Inc. — FEI 3006646024

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