FDA Inspection 860090 — LKC Technologies, Inc.

LKC Technologies, Inc. — FEI 1119189

The FDA completed an inspection of LKC Technologies, Inc. on Dec 17, 2013 in Gaithersburg, MD. 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
Dec 17, 2013
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Gaithersburg, MD (United States)