FDA Inspection 754534 — Rondex Products, Inc.

Rondex Products, Inc. — FEI 1419464

The FDA completed an inspection of Rondex Products, Inc. on Nov 23, 2011 in Rockford, IL. 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 23, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Rockford, IL (United States)