FDA Inspection 740562 — Action Products Incorporated

Action Products Incorporated — FEI 1181047

The FDA completed an inspection of Action Products Incorporated on August 9, 2011 in Hagerstown, MD. 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
August 9, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hagerstown, MD (United States)