FDA Inspection 791127 — Theg, Inc.

Theg, Inc. — FEI 3006314863

The FDA completed an inspection of Theg, Inc. on June 20, 2012 in Bergenfield, 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
June 20, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Bergenfield, NJ (United States)