FDA Inspection 1228979 — Rondex Products, Inc.
The FDA completed an inspection of Rondex Products, Inc. on Jan 31, 2024 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
- Jan 31, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Rockford, IL (United States)