FDA Inspection 820109 — Elk Industries Inc

Elk Industries Inc — FEI 3005327395

The FDA completed an inspection of Elk Industries Inc on Feb 25, 2013 in Melbourne, FL. 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 25, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Melbourne, FL (United States)