FDA Inspection 544652 — Interlectric Corporation

Interlectric Corporation — FEI 2523544

The FDA completed an inspection of Interlectric Corporation on October 21, 2008 in Warren, PA. 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
October 21, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Warren, PA (United States)