FDA Inspection 696606 — Segami Corporation

Segami Corporation — FEI 3003370689

The FDA completed an inspection of Segami Corporation on Nov 4, 2010 in Columbia, 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
Nov 4, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbia, MD (United States)