FDA Inspection 620022 — Theg, Inc.

Theg, Inc. — FEI 3006314863

The FDA completed an inspection of Theg, Inc. on October 13, 2009 in Bergenfield, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 13, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Bergenfield, NJ (United States)