FDA Inspection 868209 — AML Distribution

AML Distribution — FEI 3010660050

The FDA completed an inspection of AML Distribution on January 25, 2014 in Hackensack, NJ. 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
January 25, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Hackensack, NJ (United States)