FDA Inspection 712741 — Alltrade Inc.

Alltrade Inc. — FEI 1000254182

The FDA completed an inspection of Alltrade Inc. on February 9, 2011 in Long Beach, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Long Beach, CA (United States)