FDA Inspection 807661 — G.T. Laboratories, Inc.

G.T. Laboratories, Inc. — FEI 1419801

The FDA completed an inspection of G.T. Laboratories, Inc. on Nov 14, 2012 in Lisle, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 14, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lisle, IL (United States)