FDA Inspection 653699 — Camlog Usa

Camlog Usa — FEI 3004433109

The FDA completed an inspection of Camlog Usa on Mar 25, 2010 in Indianapolis, IN. 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
Mar 25, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Indianapolis, IN (United States)