FDA Inspection 821024 — LGC Clinical Diagnostics, Inc.

LGC Clinical Diagnostics, Inc. — FEI 3003407015

The FDA completed an inspection of LGC Clinical Diagnostics, Inc. on Feb 7, 2013 in Cumberland Foreside, ME. 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
Feb 7, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Cumberland Foreside, ME (United States)